Harry S. Paris A.R.O., Newe Ya'ar Research Center, Ramat Yishay 30-095 (Israel)
Eileen Kabelka University of Florida, Gainesville, Fl 32611 (U.S.A.)
The genus Cucurbita L. contains 12 or 13 species (50). As far as is known, all have a complement of 20 pairs of chromosomes (2n = 40).
This gene list for Cucurbita contains detailed sources of information, being modeled after the one for cucumber presented by Wehner and Staub (103) and its update by Xie and Wehner (109). In order to more easily allow confirmation of previous work and as a basis for further work, information has been included concerning the genetic background of the parents that had been used for crossing. Thus, in addition to the species involved, the cultivar-group (for C. pepo), market type (for C. maxima, C. moschata), and/or cultivar name are included in the description wherever possible.
Genes affecting phenotypic/morphological traits are listed in Table 1. The data upon which are based identifications and concomitant assignment of gene symbols vary considerably in their content. No attempt is made here to assess the certainty of identifications, but gene symbols have been accepted or assigned only for cases in which at least some data are presented. The genes that are protein/isozyme variants are listed in Table 2. It can be seen from Tables 1 and 2 that approximately 70 genes have been identified for C. pepo L, for C. moschata Duchesne 25 and for C. maxima Duchesne 19. For the interspecific cross of C. maxima × C. ecuadorensis Cutler & Whitaker, 29 genes have been identified, of which 25 are isozyme variants. A few genes have also been identified in four of the wild species (C. okeechobeensis Bailey, C. lundelliana Bailey, C. foetidissima HBK and C. ecuadorensis) and in several other interspecific crosses.
Some genes are listed as occurring in more than one species. This does not necessarily indicate that these genes reside at identical locations in the genome of different species.
New additions to the list of Cucurbita genes include a number of omissions as well as a number of new genes published after the last update. Those that had been omitted are three unnamed genes for fruit bitterness (3). They are herein designated Bitter fruit-1, -2, and -3, symbols Bi-1, Bi-2, and Bi-3. This has necessitated the modification of the symbols for the two previously identified genes (12, 30, 32) for Bitter fruit as Bimax and Bi-0. Newly identified genes that have been published since the last update are: ae (androecy enhancer), Crr-1, Crr-2, and Crr-3 (Crown rot resistance-1, -2, and -3), gl-2 (glabrous-2), and l-2R (light type-2 Reverse striping). The symbols ae, Crr-1, Crr-2, and Crr-3 are herein assigned for the first time. Before choosing a gene name and symbol, researchers are urged to consult this Gene List as well as the rules of Gene Nomenclature for the Cucurbitaceae that appears near the end of this Cucurbit Genetics Cooperative Report in order to avoid confusion arising from duplication of gene names and symbols. Please contact us if you find omissions or errors in this Gene List.
Several cases of genetic linkage have been reported: D – mo-2 (61) and M – Wt (C. pepo) (72) and Bi – Lo-2 (C. ecuadorensis × C. maxima) (32). Some of the isozyme variants observed by Weeden & Robinson (102) were also found to be linked to one another. RAPD markers have been categorized and organized into linkage groups and are not listed here but can be found in Brown and Myers (5) and Zraidi and Lelley (111). These two maps cannot be easily compared, as they were constructed using different mapping populations; RAPD markers are population-specific. Neither map gives complete coverage of the Cucurbita genome. Both maps contain morphological traits, either as single genes or as quantitative trait loci (QTLs), which are listed in Table 3. More recently, a map for Cucurbita pepo has been constructed using RAPDs, AFLPs, and SSRs (27, 113). Over 300 markers were mapped, with coverage of some 2,200 cM of the genome, 20 linkage groups and a map density of 2.9 cM.
Sequenced genes can be valuable to breeders and geneticists, as the differences in the gene sequences that result in the phenotypes of interest can be used in marker-assisted selection. Unlike random markers, these gene-specific, allele-specific markers are completely linked to the genes of interest. Most of the genes sequenced in Cucurbita have been isolated by researchers doing comparative studies of specific genes across plant families; usually only a single allele is available. Nonetheless, we have included a list of the sequenced genes as Table 4 because the sequences could be useful as a starting point for breeders interested in isolating the genes from lines of differing phenotype. In addition to the genes listed here, there exists a collection of partial sequences from mRNA for genes differentially expressed during seed development in C. pepo. These expressed sequence tags were identified in a study of the naked seed trait. The Gene Accession numbers for these sequences are CD726806 through CD726832.
Table 1. Phenotypic/Morphological Characteristics
Gene Symbol |
|
|
|
Preferred |
Synonym |
Character |
Species |
Reference(s) |
a |
|
androecious. Found in ‘Greckie’; produces only male flowers, recessive to A. |
pepo |
41 |
ae* |
|
androecy enhancer. From cross between two vegetable-marrow cultivars, the strongly male ‘Vegetable Spaghetti’, ae/ae , and ‘Bolognese’, Ae/Ae. |
pepo |
48 |
B |
|
Bicolor. Precocious yellow fruit pigmentation; pleiotropic, affecting fruit and foliage, modified by Ep-1, Ep-2 and Ses-B. Originally from ‘Vaughn’s Pear Shaped’ ornamental gourd. B in C. moschata ‘Precocious PI 165561’ derived from C. pepo through backcrossing. Complementary to L-2 for intense orange, instead of light yellow, fruit-flesh color. |
pepo, moschata |
57, 74, 84, 91, 93 |
Bmax |
B-2 |
Bicolor. Precocious yellow fruit pigmentation, from subsp. andreana PI 165558 |
maxima |
92, 95 |
Bimax* |
Bi |
Bitter fruit. High cucurbitacin content in fruit. Bi from C. maxima subsp. andreana and C. ecuadorensis; bi from C. maxima subsp. maxima, including ‘Queensland Blue’. Linked to Lo-2. |
maxima, maxima × ecuadorensis |
12, 32 |
Bi-0 * |
Bi |
Bi-0 from wild Texan gourd; bi-0 from zucchini squash. Might be identical with either Bi-1 or Bi-2. |
pepo |
30 |
Bi-1 * |
|
In cross of C. pepo ×C. argyrosperma, three complementary dominant alleles are needed for bitterness. Bi-1 from C. pepo straightneck ‘Goldbar’, bi-1 from C. argyrosperma ‘Green Striped Cushaw’. |
pepo × argyrosperma |
3 |
Bi-2 * |
|
In cross of C. pepo ×C. argyrosperma, three complementary dominant alleles are needed for bitterness. Bi-2 from C. pepo straightneck ‘Goldbar’, bi-2 from C. argyrosperma ‘Green Striped Cushaw’. |
pepo × argyrosperma |
3 |
Bi-3 * |
|
In cross of C. pepo ×C. argyrosperma, three complementary dominant alleles are needed for bitterness. Bi-3 from C. argyrosperma ‘Green Striped Cushaw’, bi-3 from C. pepo straightneck ‘Goldbar’. |
pepo × argyrosperma |
3 |
bl |
|
blue fruit color. Incompletely recessive to Bl forgreen fruit color, in hubbard squash. |
maxima |
33 |
Bn |
|
Butternut fruit shape, from ‘New Hampshire Butternut’, dominant to bn for crookneck fruit shape, as in ‘Canada Crookneck’. |
moschata |
52 |
Bu |
D |
Bush habit. Short internodes; dominant to vine habit, bu, in young plant stage. In C. pepo, Bu in ‘Giant Yellow Straightneck’ and near-isogenic line of ‘Table Queen’, bu in ‘Table Queen’ acorn. In C. maxima, Bu from inbred line, bu from ‘Delicious’. In C. moschata, Bu from inbred line, bu from undisclosed parent. |
pepo, maxima, moschata |
18, 31, 90, 106 |
Cmv |
|
Cucumber mosaic virus resistance, from Nigerian Local. Dominant to cmv for susceptiblity, from ‘Waltham Butternut’. |
moschata |
4 |
cr |
|
cream corolla. Cream to nearly white petals, cr from C. okeechobeensis; Cr from C. moschata ‘Butternut’ incompletely dominant (yellow petals for Cr/cr, and orange for Cr/Cr) |
moschata × okeechobeensis |
81 |
Crr-1* |
|
Crown rot resistance. Resistance to Phytophthora capsici, introgressed from C. lundelliana and C. okeechobeensis subsp. okeechobeensis into a breeding line of C. moschata. One of three complementary dominant genes for resistance. Genotype of the susceptible C. moschata ‘Butterbush’ is crr-1/crr-1. |
moschata |
56 |
Crr-2* |
|
Crown rot resistance. Resistance to Phytophthora capsici, introgressed from C. lundelliana and C. okeechobeensis subsp. okeechobeensis into a breeding line of C. moschata, One of three complementary dominant genes for resistance. Genotype of the susceptible C. moschata ‘Butterbush’ is crr-2/crr-2. |
moschata |
56 |
Crr-3* |
|
Crown rot resistance. Resistance to Phytophthora capsici, introgressed from C. lundelliana and C. okeechobeensis subsp. okeechobeensis into a breeding line of C. moschata. One of three complementary dominant genes for resistance. Genotype of the susceptible C. moschata ‘Butterbush’ is crr-3/crr-3. |
moschata |
56 |
cu |
|
cucurbitacin-B reduced; cu for reduced cucurbitacin-B content of cotyledons of ‘Early Golden Bush Scallop’; Cu for high cucurbitacin content of cotyledons of ‘Black Zucchini’. |
pepo |
89 |
D |
|
Dark stem. Series of three alleles observed in C. pepo: D for dark stem and dark intermediate-age fruit, Ds for dark stem but fruit not affected, and d for light stem and fruit not affected, with dominance D > Ds > d. D from ‘Fordhook Zucchini’, Ds from ‘Early Prolific Straightneck’; d from ‘Vegetable Spaghetti’. Epistatic to genes l-1 and l-2 when either is homozygous recessive; linked to mo-2. In C. maxima, only the fruit was observed: D for dark intermediate-age fruit from the zapallito ‘La Germinadora’; d for light intermediate-age fruit from a variant zapallito breeding stock. |
pepo, maxima |
26, 45, 60, 61, 64, 73, 86 |
de |
|
determinate plant habit; stem lacking tendrils and terminating with female flowers. Recessive to De for indeterminate plant habit. De from ‘Jeju’ and ‘Sokuk’, de from inbred designated “Det”. |
moschata |
42 |
Di |
|
Disc fruit shape. From scallop squash, dominant to spherical or pyriform. |
pepo |
97, 104 |
Ep-1 |
|
Extender of pigmentation-1; modifier of B. Ep-1 incompletely dominant to ep-1 and additive with Ep-2. Ep-1 from ‘Small Sugar 7 × 7’ pumpkin; ep-1 from ‘Table King’ acorn. |
pepo |
96 |
Ep-2 |
|
Extender of pigmentation-2; modifier of B. Ep-2 incompletely dominant to ep-2 and additive with Ep-1. Ep-2 from ‘Table King’ acorn; ep-2 from ‘Small Sugar 7 × 7’ pumpkin. |
pepo |
96 |
Fr |
|
Fruit fly (Dacus cucurbitae) resistance. Fr from ‘Arka Suryamukhi’, dominant to fr forsusceptibility. |
maxima |
53 |
fv |
|
fused vein. Fusion of primary leaf veins, subvital male gametophyte; found in hull-less-seeded pumpkin breeding line. |
pepo |
8, 9 |
G |
a, m |
Gynoecious sex expression; dominant to g for monoecious sex expression. |
foetidissima |
19, 24 |
Gb |
|
Green band on inner side of base of petal, from a scallop squash; dominant to gb, for no band, from a straightneck squash. |
pepo |
20 |
gc |
|
green corolla. Green, leaf-like petals, sterile; in unspecified F2 population. |
pepo |
99 |
gl-1* |
gl |
glabrous, lacking trichomes |
maxima |
37 |
gl-2 |
|
glabrous, lacking trichomes; gl-2 mutant found in straightneck squash |
pepo |
108 |
Gr |
G |
Green rind. Dominant to buff skin of mature fruit. Gr from ‘Long Neapolitan’, gr from ‘Butternut’. |
moschata |
77 |
grl |
|
gray leaf. Recessive to green leaf. Recessive grl derived from cross of zapallito-type line of C. maxima and a butternut-type line of C. moschata. Dominant Grl from zapallito-type C. maxima. |
maxima × moschata |
44 |
Hi |
|
Hard rind inhibitor. Hi, for hard-rind inhibition, from C. maxima ‘Queensland Blue’; hi, for no hard-rind inhibition, from C. ecuadorensis. |
maxima × ecuadorensis |
30 |
Hr |
|
Hard rind. Hr for hard (lignified) rind inornamental gourd, straightneck squash, and zucchini; hr for soft (non-lignified) rind in ‘Small Sugar’ pumpkin and ‘Sweet Potato’ (‘Delicata’). Complementary to Wt for Warty fruit. |
pepo |
47, 85 |
i |
|
intensifier of the cr gene for cream flowers. Cr/__ I/__ for intense orange or yellow flowers, Cr/__ i/i for light orange or yellow flowers, cr/cr I/__ for cream flowers, cr/cr i/i for white flowers. I from C. moschata ‘Butternut’, i from C. okeechobeensis. |
moschata × okeechobeensis |
81 |
I-mc |
Imc |
Inhibitor of mature fruit color; dominant to i-mc for no inhibition. I-mc in a scallop squash. |
pepo |
10 |
I-T |
|
Inhibitor of the T gene for trifluralin resistance. I-T from ‘La Primera’; i-t from ‘Ponca’ and ‘Waltham Butternut’. |
moschata |
1 |
l-1 |
c, St |
light fruit coloration-1. Light intensity of fruit coloration. Series of five alleles observed in C. pepo which, in complementary interaction with the dominant L-2 allele, give the following results: L-1 for uniformly intense/dark fruit coloration, from ‘Fordhook Zucchini’; l-1BSt for broad, contiguous intense/dark stripes, from ‘Cocozelle’; l-1St for narrow, broken intense/dark stripes, from ‘Caserta’; l-1iSt for irregular intense/dark stripes, from ‘Beirut’ vegetable marrow; l-1 for light coloration, from ‘Vegetable Spaghetti’, with dominance of L-1 > (l-1BSt > l-1St) ≥ l-1iSt > l-1. In C. maxima, L-1 from the zapallito ‘La Germinadora’; l-1 from a variant zapallito breeding stock. |
pepo, maxima |
26, 45, 62, 67, 63, 67, 73, 82, 91 |
l-2 |
r |
light fruit coloration-2. Light intensity of fruit coloration. Series of four alleles observed in C. pepo, which, in complementary interaction with dominant alleles at the l-1 locus, give the following results: L-2 for intense/dark fruit coloration, with L-1 from ‘Fordhook Zucchini’ and intense/dark fruit stripes, with l-1BSt from ‘Cocozelle’; allele L-2w has delayed and weaker effect than L-2, from C. pepo subsp. fraterna; l-2R confers reversal of color, that is, stripes lighter than the background in combination with any of the striping alleles at the l-1 locus, or completely light fruit in the presence of L-1, from C. pepo subsp. texana ‘Delicata’; l-2 for light coloration, from ‘Vegetable Spaghetti’, with dominance of L-2 > L-2w > l-2. Dominant L-2 is also complementary with B for intense orange, instead of light yellow, fruit-flesh color and with recessive qi for intense exterior color of young fruit. In C. maxima, L-2 from the zapallito ‘La Germinadora’; l-2 from a variant zapallito breeding stock. |
pepo, maxima |
26, 45, 57, 65, 68, 69, 73 |
lo-1 |
l |
lobed leaves-1; recessive to Lo-1 for non-lobed leaves |
maxima |
21 |
Lo-2 |
|
Lobed leaves-2. Lo-2 for lobed leaves in C. ecuadorensis dominant to lo-2 for unlobed leaves in C. maxima. Linked to Bi. |
ecuadorensis × maxima |
32 |
lt |
|
leafy tendril. Tendrils with laminae; lt found in ornamental gourd. |
pepo |
83 |
ly |
|
light yellow corolla. Recessive to orange yellow; ly found in ornamental gourd. |
pepo |
83 |
M |
|
Mottled leaves. M for silver-gray areas in axils of leaf veins, dominant to m for absence of silver-gray. For C. maxima, M in ‘Zuni’ and m in ‘Buttercup’ and ‘Golden Hubbard’. For C. pepo, M in ‘Caserta’ and inbred of ‘Striato d’Italia’ cocozelle; m in ‘Early Prolific Straightneck’ and ‘Early Yellow Crookneck’. For C. moschata, M in ‘Hercules’ and ‘Golden Cushaw’, m in butternut type. Weakly linked to Wt. |
pepo, maxima, moschata |
14, 66, 82, 87 |
Mldg |
|
Mottled light and dark green immature fruit color; germplasm unspecified. Dominant to mldg for non-mottled. |
moschata |
6 |
mo-1 |
|
mature orange-1; complementary recessive gene for loss of green fruit color prior to maturity. Mo-1 from ‘Table Queen’ acorn; mo-1 from ‘Vegetable Spaghetti’. |
pepo |
61 |
mo-2 |
|
mature orange-2; complementary recessive gene for loss of green fruit color prior to maturity. Mo-2 from ‘Table Queen’ acorn; mo-2 from ‘Vegetable Spaghetti’. Linked to D. |
pepo |
61 |
ms-1 |
ms1 |
male sterile-1. Male flowers abort before anthesis, derived from a cross involving ‘Golden Hubbard’, recessive to Ms-1 for male fertile. |
maxima |
88 |
ms-2 |
ms2 |
male sterile-2. Male flowers abort, sterility expressed as androecium shrivelling and turning brown; ms-2 from ‘Eskandarany’ (PI 228241). |
pepo |
23 |
ms-3 |
ms-2 |
male sterile-3. |
maxima |
39 |
m-zymmos |
|
modifier of dominance of zucchini yellow mosaic virus resistance; confers resistance to otherwise susceptible Zymmos/zymmos heterozygotes. M-zymmos in ‘Soler’, m-zymmos in ‘Waltham Butternut’ and ‘Nigerian Local’. |
moschata |
55 |
n |
h |
naked seeds. Lacking a lignified seed coat, n from oil-seed pumpkin. |
pepo, moschata |
29, 86, 107, 112, 113 |
pl |
|
plain light fruit color, pl from ‘Beirut’ vegetable marrow and ‘Fordhook Zucchini’; Pl in ‘Vegetable Spaghetti’. |
pepo |
58 |
Pm |
|
Powdery mildew resistance. Resistance to Podosphaera xanthii; Pm from C. lundelliana. |
lundelliana |
13, 70 |
Pm-0 |
|
Powdery mildew resistance. Resistance to Podosphaera xanthii; Pm-0 from C. okeechobeensis and in C. pepo. |
okeechobeensis, pepo |
11, 37 |
pm-1 |
|
powdery mildew resistance in C. moschata. Series of three alleles: pm-1P for susceptibility from ‘Ponca’ dominant to pm-1L for resistance from ‘La Primera’, which is dominant to pm-1W for susceptibility in ‘Waltham Butternut’. |
moschata |
2 |
pm-2 |
|
powdery mildew resistance in C. moschata ‘Seminole’, recessive to Pm-2 for susceptibility |
moschata |
2 |
prv |
|
papaya ringspot virus resistance, in Nigerian Local, recessive to Prv for susceptibility, in ‘Waltham Butternut’. |
moschata |
4 |
qi |
|
quiescent intense. Recessive to Qi for not intense and complementary to L-2 for intense young fruit color; little or no effect on mature fruit. Qi from ‘Vegetable Spaghetti’; qi from ‘Jack O’Lantern’ pumpkin and ‘Verte non-coureuse d’Italie’ cocozelle. |
pepo |
63, 66 |
Rd |
|
Red skin. Red external fruit color; dominant to green, white, yellow and gray. Rd from ‘Turk’s Cap’; rd from ‘Warted Hubbard’. |
maxima |
46 |
ro |
|
rosette leaf. Lower lobes of leaves slightly spiraled, ro derived from an ornamental gourd. |
pepo |
47 |
s-1 |
s |
sterile. Male flowers small, without pollen; female flower sterile. Derived from crossing ‘Greengold’ with ‘Banana’. |
maxima |
34 |
s-2 |
|
sterile. Male flowers small, without pollen and female flower sterile; mutant in powdery mildew resistant, straightneck squash breeding line. |
pepo |
7 |
Ses-B |
|
Selective suppression of gene B. Suppression in foliage of precocious yellowing conferred by B. Ses-B in straightneck breeding line dominant to ses-B in ‘Jersey Golden Acorn’. |
pepo |
94 |
sl |
|
silverleaf resistance. Recessive to Sl for susceptibility. In C. moschata, Sl from ‘Soler’; sl from PI 162889 and butternut types. In C. pepo, Sl from ‘Black Beauty’ zucchini and sl from Zuc76 breeding line. |
moschata, pepo |
28, 110 |
slc |
|
Squash leaf curl virus resistance; derived from C. moschata. |
pepo |
50 |
sp |
|
spaghetti flesh, breaking into strands after cooking |
pepo |
49 |
T |
|
Trifluralin resistance. Dominant to susceptibility to the herbicide; modified by I-T. T in ‘La Primera’; t in ‘Ponca’ and ‘Waltham Butternut’. |
moschata |
1 |
uml |
|
umbrella-like; leaves shaped like partially opened umbrella. Recessive uml derived from a cross of C. maxima ‘Warzywna’ and a C. pepo inbred; dominant Uml from ‘Warzywna’. |
maxima × pepo |
75 |
v |
|
virescent. Yellow-green young leaves, v found in ‘Golden Delicious’. |
maxima |
22 |
W |
|
Weak fruit coloration. Dominant to w for intense-pigmented mature fruit; W from scallop squash. Complementary to Wf for white external fruit color. |
pepo |
59, 91, 97 |
wc |
|
white corolla. Derived from ‘Ispanskaya’ × ‘Emerald’. Recessive to Wc for normal orange-yellow corolla |
maxima |
40 |
Wf |
|
White flesh. Dominant to wf for colored flesh. Wf in a scallop squash, wf in a straightneck squash. Complementary to W for white external fruit color. |
pepo |
20, 59, 97 |
Wmv |
|
Watermelon mosaic virus resistance. From “Menina” and “Nigerian Local”, dominant to wmv for susceptibility in ‘Musquée de Provence’ and ‘Waltham Butternut’. May be linked with or identical to Zym-1. |
moschata |
4, 24 |
Wmvecu |
|
Watermelon mosaic virus resistance. From C. ecuadorensis, in a cross with an unspecified C. maxima. |
maxima x ecuadorensis |
95 |
Wt |
|
Warty fruit. Dominant to non-warted, wt, and complementary to Hr, with fruit wartiness being expressed only in the presence of the dominant Hr allele. Wt in straightneck, crookneck, and ‘Delicata’; wt in zucchini, cocozelle, and ‘Small Sugar’ pumpkin. Weakly linked to M. |
pepo |
66, 79, 97 |
wyc |
|
white-yellow corolla; isolated in ‘Riesen-Melonen’. Recessive to Wyc for normal orange-yellow corolla. |
maxima |
40 |
Y |
|
Yellow fruit color. Y for yellow fruit color of intermediate-age fruits, from straightneck and crookneck squash, dominant to y for green intermediate-age fruit color, from vegetable marrow, ornamental gourd, and cocozelle. |
pepo |
72, 82, 90, 91, 97 |
yg |
|
yellow-green leaves and stems |
maxima |
39 |
Ygp |
|
Yellow-green placenta. Dominant to yellow placental color. Ygp in a scallop squash, ygp in a straightneck squash. |
pepo |
20 |
ys |
|
yellow seedling. Lacking chlorophyll; lethal |
pepo |
47 |
zymecu |
|
zucchini yellow mosaic virus resistance, recessive to susceptibility; zymecu from C. ecuadorensis, Zymecu from C. maxima ‘Buttercup’. |
ecuadorensis |
80 |
zymmos |
|
zucchini yellow mosaic virus resistance, recessive to susceptibility; zym?mos from ‘Soler’, Zymmos from ‘Waltham Butternut’. |
moschata |
55 |
Zym-0 |
|
Zucchini yellow mosaic virus resistance. Zym-0 from C. moschata ‘Nigerian Local’ dominant to zym-0 for susceptibility from ‘Waltham Butternut’. Perhaps one of two separate genes for resistance in ‘Nigerian Local’. |
moschata |
4, 47, 55 |
Zym-1 |
|
Zucchini yellow mosaic virus resistance. Zym-1 from C. moschata ‘Menina’dominant to zym-1 forsusceptibility from C. moschata ‘Waltham Butternut’. Zym-1 transferred via backcrossing to C. pepo ‘True French’ zucchini, in which it confers resistance through complementary interaction with Zym-2 and Zym-3. Zym-1 is either linked with Wmv or also confers resistance to watermelon mosaic virus. |
moschata, pepo |
24, 55, 70, 71 |
Zym-2 |
|
Zucchini yellow mosaic virus resistance-2. Dominant to susceptibility and complementary to Zym-1. Zym-2 from C. moschata ‘Menina’. Zym-2 in C. pepo derived from C. moschata, in near-isogenic resistant line of ‘True French’ zucchini; zym-2 from C. pepo ‘True French’. |
moschata, pepo |
70 |
Zym-3 |
|
Zucchini yellow mosaic virus resistance-3. Dominant to susceptibility and complementary to Zym-1. Zym-3 from C. moschata ‘Menina’. Zym-3 in C. pepo derived from C. moschata, in near-isogenic resistant line of ‘True French’ zucchini; zym-3 from C. pepo ‘True French’. |
moschata, pepo |
70 |
*Proposed new gene symbol.
Table 2. Isozyme Variants
Gene Symbol |
|
|
|
|
Preferred |
Synonym |
No. alleles observed |
Character |
Species |
Reference(s) |
Aat-1 |
Aat |
8 |
Aspartate aminotransferase-1. Variant among accessions. |
pepo |
17, 36 |
Aat-3 |
|
2 |
Aspartate aminotransferase-3. Variant among wild populations. |
pepo |
17 |
Aat-4 |
|
3 |
Aspartate aminotransferase-4. Variant among wild populations. |
pepo |
17 |
Aat-mb |
|
2 |
Aspartate aminotransferase – microbody |
maxima x ecuadorensis |
102 |
Aat-m1 |
|
2 |
Aspartate aminotransferase mitochondria-1 |
maxima x ecuadorensis |
102 |
Aat-m2 |
|
2 |
Aspartate aminotransferase mitochondria-2 |
maxima x ecuadorensis |
102 |
Aat-p2 |
|
2 |
Aspartate aminotransferase plastid-2 |
maxima x ecuadorensis |
102 |
Acp-1 |
|
2 |
Acid phosphatase-1 |
maxima x ecuadorensis |
102 |
Acp-2 |
|
2 |
Acid phosphatase-2 |
maxima x ecuadorensis |
102 |
Adh |
|
2 |
Alcohol dehydrogenase |
pepo |
105 |
Aldo-p |
|
2 |
Aldolase – plastid |
maxima x ecuadorensis |
101 |
Est-1 |
Est |
2 |
Esterase |
maxima x ecuadorensis |
100, 102 |
Gal-1 |
|
2 |
b-galactosidase-1 |
maxima x ecuadorensis |
102 |
Gal-2 |
|
2 |
b-galactosidase-2 |
maxima x ecuadorensis |
102 |
G2d-1 |
|
3 |
Glycerate dehydrogenase-1. Variant among wild populations. |
pepo |
17 |
G2d-2 |
|
2 |
Glycerate dehydrogenase-2. Variant among wild populations. |
pepo |
17 |
Got-1 |
|
5 |
Glutamine oxaloacetate-1. Variant among accessions, wild populations, and among Cucurbita species. |
pepo |
15, 16, 38, 105 |
Got-2 |
|
3 |
Glutamine oxaloacetate-2. Variant among species. |
maxima x ecuadorensis |
102 |
Gpi |
|
2 |
Glucosephosphate isomerase. Variant among accessions. |
pepo |
36 |
Gpi-3 |
|
2 |
Glucosephosphate isomerase-3. Variant among wild populations. |
pepo |
17 |
Gpi-c1 |
|
2 |
Glucosephosphate isomerase cytosolic-1 |
maxima x ecuadorensis |
102 |
Gpi-c2 |
|
2 |
Glucosephosphate isomerase cytosolic-2 |
maxima x ecuadorensis |
102 |
Idh-1 |
|
4 |
Isocitrate dehydrogenase-1. Variant among accessions, wild populations, and Cucurbita species. |
pepo |
15, 16, 17, 38, 105 |
Idh-2 |
|
2 |
Isocitrate dehydrogenase-2. Variant among accessions, wild populations, and Cucurbita species. |
pepo |
15, 16, 17, 38, 105 |
Idh-3 |
|
2 |
Isocitrate dehydrogenase-3. Variant among accessions and populations. |
pepo |
15, 16, 17, 38 |
Lap-1 |
Lap |
4 |
Leucine aminopeptidase. Variant among C. pepo accessions. |
maxima x ecuadorensis; pepo |
17, 36, 100, 102 |
Mdh-1 |
Mdh |
7 |
Malate dehydrogenase. Variant among accessions. |
pepo |
36 |
Mdh-2 |
|
3 |
Malate dehydrogenase-2. Variant among accessions, wild populations, and Cucurbita species. |
pepo |
15, 16, 17, 38, 105 |
Mdh-3 |
|
3 |
Malate dehydrogenase-3. Variant among accessions, wild populations, and Cucurbita species. |
pepo |
15, 16, 17, 38, 105 |
Mdh-m1 |
|
2 |
Malate dehydrogenase mitochondria-1 |
maxima x ecuadorensis |
102 |
Mdh-m2 |
|
2 |
Malate dehydrogenase mitochondria-2 |
maxima x ecuadorensis |
102 |
Mdh-c2 |
|
2 |
Malate dehydrogenase cytosolic-2 |
maxima x ecuadorensis |
102 |
Per-1 |
|
2 |
Peroxidase-1 |
maxima x ecuadorensis |
102 |
Per-2 |
|
3 |
Peroxidase-2. Variant among accessions and wild populations. |
pepo |
15, 16, 38 |
Per-3 |
|
2 |
Peroxidase-3 |
maxima x ecuadorensis |
102 |
Pgi-1 |
|
2 |
Phosphoglucase isomerase-1 |
pepo |
15 |
Pgi-2 |
|
2 |
Phosphoglucase isomerase-2. Variant among Cucurbita species. |
pepo |
15, 38, 105 |
Pgi-3 |
|
4 |
Phosphoglucase isomerase-3. Variant among accessions, wild populations, and Cucurbita species. |
pepo |
15, 16, 38, 105 |
Pgm-1 |
Pgm |
2 |
Phosphoglucomutase. Variant among accessions. |
pepo |
36 |
Pgm-2 |
|
4 |
Phosphoglucomutase-2. Variant among accessions, wild populations, and Cucurbita species. |
pepo |
15, 16, 38, 105 |
Pgm-5 |
|
2 |
Phosphoglucomutase-5. Variant among wild populations. |
pepo |
17 |
Pgm-6 |
|
2 |
Phosphoglucomutase-6. Variant among wild populations. |
pepo |
17 |
Pgm-c2 |
|
2 |
Phosphoglucomutase cytosolic-2 |
maxima x ecuadorensis |
102 |
Pgm-p |
|
2 |
Phosphoglucomutase plastid |
maxima x ecuadorensis |
102 |
Skd-1 |
|
6 |
Shikimate dehydrogenase. Variant among wild populations. |
pepo |
17 |
Skdh |
|
5 |
Shikimate dehydrogenase. Variant among C. pepo accessions. |
maxima x ecuadorensis; pepo |
36, 102 |
Sod-1 |
|
2 |
Superoxide dismutase-1 |
maxima x ecuadorensis |
102 |
Tpi-c2 |
|
2 |
Triosephosphatase isomerase cytosolic-2 |
maxima x ecuadorensis |
102 |
Tpi-p2 |
|
2 |
Triosephosphatase isomerase plastid-2 |
maxima x ecuadorensis |
102 |
Table 3. Mapped Phenoypic/Morphological Characteristics
Trait |
Symbol |
Linked Marker(s) |
Recombination Distance (cM) |
Reference(s) |
Precocious yellow fruit |
B |
I10_1700 |
27.1 |
5 |
Bush growth habit |
Bu |
CMTp131 |
7.8 |
27 |
Dwarf |
Bu |
S1225_548, SCAR3_398 |
2.29 |
43 |
Leaf Mottle |
M |
H14_600 U489_1200 |
13.0 16.3 |
5 |
Seed Coat |
n |
AK11_340 |
4.4 |
111 |
Hull-less seed |
n |
CMTp58, CMTp151, CMTm115, CMTm239 |
1.5 - 3.6 |
27 |
Mature Fruit Color |
[none given] |
G17_700 |
9.7 |
5 |
Fruit Length |
(QTL) |
AE07_165, AC10_490, AJ20_420, P13_750, J01_600, AO20_1200, T08_460, AB08_540, AE09_1600 |
|
111 |
Fruit Width |
(QTL) |
AE07_165, AJ20_420, AM10_950, AG08_440 |
|
111 |
Fruit Length/width Ratio |
(QTL) |
AE07_165, AC10_490, AJ20_420, P13_750, J01_600 |
|
111 |
No. of Fruit Chambers |
(QTL) |
P13_950, AE08_470 |
|
111 |
Leaf Indentation |
(QTL) |
F10_400, K11_950, G2_400 |
|
5 |
Fruit Shape |
(QTL) |
F8_1050, B8_900, H19_500 |
|
5 |
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- Whitaker, T.W. 1932. Fertile gourd-pumpkin hybrids. J. Hered. 23: 427–430.
- Wilson, H.D. 1989. Discordant patterns of allozyme and morphological variation in Mexican Cucurbita. Syst. Bot. 14: 612–623.
- Wu, T., J. Zhou, Y. Zhang, and J. Cao. 2007. Characterization and inheritance of a bush-type in tropical pumpkin (Cucurbita moschata Duchesne). Sci. Hort. 114: 1–4.
- Xianglin, Z. 1987. A study on the breeding of naked kernel pumpkin and its genetic behavior. Acta Hort. Sin. 14: 115–118 (Chinese, with English summary).
- Xiao, Q. and J.B. Loy. 2007. Inheritance and characterization of a glabrous trait in summer squash. J. Amer. Soc. Hort. Sci. 132: 327–333.
- Xie, J. and T.C. Wehner. 2001. Gene list 2001 for cucumber. Cucurbit Genet. Coop. Rep. 24: 110–136.
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- Zraidi, A., M. Pachner, T. Lelley, and R. Obermayer. 2003. On the genetics and histology of the hull-less character of Styrian oil-pumpkin (Cucurbita pepo L.). Cucurbit Genet. Coop. Rep. 26: 57–61.
- Zraidi, A., G. Stift, M. Pachner, A. Shojaeiyan, L. Gong, and T. Lelley. 2007. A consensus map for Cucurbita pepo. Mol. Breed. 20: 375–388.
Table 4. Genes with known DNA sequence.
Gene Symbol* |
Gene Accession |
(Putative) Function |
Source |
Ref. |
AIG-2 |
AY666083 |
aspartic protease inhibitor |
C. maxima |
** |
PRB1 |
AY326308 |
phloem RNA-binding protein |
C. maxima ‘Big Max’ |
** |
GAIP |
AY32630, AY326307 |
gibberellic acid insensitive phloem protein (two very similar genes) |
C. maxima ‘Big Max’ |
** |
FAD2 |
AY525163 |
omega-6 fatty acid desaturase |
C. pepo zucchini |
** |
NIP1 |
AJ544830 |
Nod26-like protein |
C. pepo zucchini |
35 |
PP2 |
AY312402 |
phloem protein 2 lectin (includes promoter region) |
C. moschata crookneck |
** |
PP2 |
AF150627 |
phloem protein 2 lectin |
C. moschata crookneck |
** |
PP2 |
Z22647 |
phloem protein 2 lectin |
C. pepo ‘Autumn Gold’ |
61 |
PP2 |
Z17331 |
phloem protein 2 lectin |
C. maxima ‘Big Max’ |
5 |
PP2 |
L31550, L31551, L31552 |
phloem protein 2 (three alleles) |
C. maxima |
** |
GA2OX, GA20OX, GA3OX |
AJ315663, AJ302041, AJ308480, AJ302040 |
gibberellin oxidases (two sequences for GA2OX) |
C. maxima ‘Riesenmelone’ |
** |
|
U61385 |
gibberellin 20-oxidase |
C. maxima ‘Riesenmelone’ |
38 |
|
U63650 |
gibberellin 2 beta,3 beta hydroxylase |
C. maxima ‘Riesenmelone’ |
39 |
|
AJ006453 |
gibberellin 3 beta hydroxylase |
C. maxima ‘Riesenmelone’ |
** |
|
U61386 |
gibberellin dioxygenase |
C. maxima ‘Riesenmelone’ |
37 |
Moschatin 1 through 5 |
AF462349, AF504011, AY25646, AY27921, AY279217 |
ribosome-inactivating protein |
C. moschata crookneck |
** |
CPS1 |
AB109763 |
copalyl diphosphate synthase; gibberellin biosynthesis |
C. maxima |
** |
CPS |
AF049905, AF049906 |
copalyl diphosphate synthase; gibberellin biosynthesis (2 genes) |
C. maxima |
55 |
Hsc70 |
AF527794, AF527795, AF527796 |
cell-autonomous heat shock protein; chaperonin 70 (multiple sequences) |
C. maxima |
1 |
|
AB061204 |
thioredoxin h |
C. maxima |
** |
Puga, Pugb, Pugc |
AB055116, AB055117, AB055118 |
glutathione S-transferase |
C. maxima |
** |
CYP88A |
AF212990, AF212991 |
cytochrome P450; ent-kaurenoic acid oxidase (multiple alleles) |
C. maxima ‘Queensland Blue’ |
23 |
PP2 |
AF520583 |
phloem protein 2 |
C. digitata PI 240879 |
** |
PP2 |
AF520582 |
phloem lectin |
C. argyrosperma subsp. sororia |
** |
|
L32700, L32701 |
phloem lectin |
C. argyrosperma |
5 |
|
X56948 |
malate synthase |
Cucurbita sp.*** ‘Kurokawa Amakuri Nankin’ |
44 |
pMCPN60 |
X70867, X70868 |
chaperonin 60 |
‘Kurokawa Amakuri Nankin’ |
59 |
PCPK |
AY07280, AY072802 |
phloem calmodulin-like protein kinases |
C. maxima ‘Big Max’ |
66 |
|
X55779 |
ascorbate oxidase |
C. maxima ‘Ebisu Nankin’ |
14 |
AAO |
D55677 |
ascorbate oxidase |
C. maxima |
33 |
chitP1 |
AB015655 |
chitinase |
C. maxima ‘Ebisu Nankin’ |
** |
PLC |
AF082284 |
chitinase |
C. moschata crookneck |
32 |
PV72 |
AB006809 |
vacuolar sorting receptor |
‘Kurokawa Amakuri Nankin’ |
54 |
|
D88420 |
stromal ascorbate peroxidase |
‘Kurokawa Amakuri Nankin’ |
42 |
|
D78256 |
isocitrate lyase |
‘Kurokawa Amakuri Nankin’ |
41 |
|
D70895 |
3-ketoacyl-CoA thiolase |
‘Kurokawa Amakuri Nankin’ |
31 |
|
D83656 |
thylakoid ascorbate peroxidase |
‘Kurokawa Amakuri Nankin’ |
64 |
|
D49433 |
hydroxypyruvate reductase |
‘Kurokawa Amakuri Nankin’ |
21 |
MP28 |
D45078 |
membrane protein |
‘Kurokawa Amakuri Nankin’ |
28 |
|
D38132 |
glyoxysomal citrate synthase |
‘Kurokawa Amakuri Nankin’ |
30 |
|
D29629 |
aconitase |
‘Kurokawa Amakuri Nankin’ |
19 |
|
D16560 |
prepro2S albumin |
‘Kurokawa Amakuri Nankin’ |
17 |
|
D14044 |
glycolate oxidase |
‘Kurokawa Amakuri Nankin’ |
58 |
|
AF002016 |
acyl CoA oxidase |
‘Kurokawa Amakuri Nankin’ |
18 |
PP36 |
AF274589 |
cytochrome b5 reductase |
C. maxima ‘Big Max’ |
** |
pAPX |
AB070626 |
peroxisomal ascorbate peroxidase |
‘Kurokawa Amakuri Nankin’ |
48 |
CM-ACS3 |
AB038559 |
ACC synthase |
C. maxima |
62 |
CmATS |
AB049135 |
acyl-(acyl-carrier protein); acyltransferase |
C. moschata ‘Shirogikuza’ |
** |
|
Y00771 |
glycerol-3-phosphate acyltransferase transit peptide |
C. moschata ‘Shirakikuza’ |
29 |
|
AB002695 |
aspartic endopeptidase |
C. pepo |
24 |
PS-1 |
AF284038 |
phloem serpin |
C. maxima |
65 |
SLW |
AF170086, AF170087 |
silverleaf whitefly-induced protein (multiple genes) |
C. pepo zucchini ‘Chefini’ |
60 |
aprX |
Y17192 |
anionic peroxidase |
C. pepo zucchini ‘Black Beauty’ |
6 |
cpCPK1 |
U90262 |
calcium-dependent calmodulin-independent protein kinase |
C. pepo zucchini |
13 |
PP16 |
AF079170, AF079171 |
mRNA movement protein; phloem transport (multiple alleles) |
C. maxima ‘Big Max’ |
63 |
AOBP |
D45066 |
transcription factor binding to ascorbate oxidase |
C. maxima |
34 |
accW |
D01032 |
auxin-induced 1-aminocyclopropane-1-carboxylate synthase |
C. maxima ‘Ebisu’ |
47 |
|
U37774 |
auxin-induced 1-aminocyclopropane-1-carboxylic acid synthase |
C. maxima |
46 |
ACC1 |
M58323 |
1-aminocyclopropane-1-carboxylate synthase |
C. pepo |
52 |
ACC1A, ACC1B |
M61195 |
1-aminocyclopropane-1-carboxylate synthase (2 genes, tightly linked) |
C. pepo zucchini |
26 |
PHP-1 |
D86306 |
proton-translocating inorganic pyrophosphatase |
C. moschata crookneck |
** |
PP1 |
U66277 |
phloem filament protein |
C. maxima ‘Big Max’ |
9 |
pfiAF4 |
X81647 |
trypsin inhibitor |
C. maxima ‘Supermarket Hybrid’ |
45 |
pfiBM7 |
X81447 |
chymotrypsin inhibitor |
C. maxima ‘Supermarket Hybrid’ |
45 |
|
M15265 |
phytochrome |
C. pepo zucchini ‘Black Beauty’ |
53 |
NADH |
M33154 |
nitrate reductase |
C. maxima |
11 |
|
M36407 |
11S globulin beta-subunit |
‘Kurokawa Amakuri Nankin’ |
20 |
|
AF206895 |
18S ribosomal RNA |
C. pepo |
** |
|
AF479108 |
26S ribosomal RNA |
C. pepo |
56 |
|
AJ488214 EF595858 FJ915115 FJ915114 FJ915113 FJ915112 FJ915111 FJ915110 FJ915109 FJ915108 FJ915107 FJ915106 FJ915105 FJ915104 FJ915101 AM981172 AM981170 AM981169 AM981168 |
5.8S ribosomal RNA |
C. moschata C. ficifolia C. pepo C. lundelliana |
**, 7 |
|
AY396415 |
5S ribosomal RNA |
C. pepo |
12 |
|
FJ263619 |
16S ribosomal RNA |
C. moschata |
** |
|
DQ298735 AY357209 AY357208 |
18S ribosomal RNA |
C. pepo C. moschata |
**,4 |
|
AF017158 |
25S ribosomal RNA |
C. maxima |
** |
GID1b |
AM745267 |
gibberellin receptor |
C. maxima |
** |
APRX |
DQ518906 |
class III peroxidase precursor |
C. pepo zucchini‘Black Beauty’ |
10 |
RBP50 |
EU793994 |
polypyrimidine tract binding protein |
C. maxima‘Big Max’ |
16 |
|
AJ829947 |
reverse transcriptase |
C. pepo |
** |
rbcL |
AF206756 L21938 DQ535804 EU309692 |
ribulose 1,5-bisphosphate carboxylase |
C. pepo C. ficifolia C. moschata |
36,57 |
NACP1 |
FJ151402 |
NAC-domain containing protein |
C. maxima |
50 |
DNCED1 |
EU391616 |
9-cis-epoxycarotenoid dioxygenase |
C. moschata |
** |
PhoH1 |
AB435244 |
alpha-1,4-glucan phosphorylase H isozyme |
C. maxima |
** |
PhoL1 |
AB435243 |
alpha-1,4-glucan phosphorylase L isozyme |
C. maxima |
** |
PP16-1 |
EU430061 |
16kDa phloem protein 1 |
C. maxima´ C. moschata ‘Ribenzhenmu’ |
** |
PP16-2 |
EU430062 |
16kDa phloem protein 2 |
C. maxima´ C. moschata ‘Ribenzhenmu’ |
** |
PP16-1 |
EF055181 |
phloem protein 1 |
C. pepo |
** |
PP16-2 |
EF055182 |
phloem protein 2 |
C. pepo |
** |
|
D01033 |
1-aminocyclopropane-1-carboxylate synthase |
C. maxima ‘Ebisu’ |
27 |
|
EF103124 |
mitochondrial alternative oxidase |
C. pepo |
** |
matK |
DQ536666 DQ536665 DQ536664 |
maturase K |
C. pepo C. digitata C. ficifolia |
36 |
trnG |
EF595908 |
tRNA-Gly |
C. pepo |
15 |
|
EF202177 |
aquaporin |
C. ficifolia |
** |
|
EU056338 |
chitinase |
C. moschata |
** |
cat1 |
D55645 |
catalase |
C. pepo |
** |
cat2 |
D55646 |
catalase |
C. pepo |
** |
cat3 |
D55647 |
catalase |
C. pepo |
** |
|
AF260737 |
catalase |
C. pepo |
** |
FTL1 |
EF462211 DQ865290 |
flowering locus T protein 1 |
C. moschata PI441726 C. maxima ‘Big Max’ |
40 |
FTL2 |
DQ865291 |
flowering locus T protein 2 |
C. maxima ‘Big Max’ |
40 |
|
AB303333 |
glyoxalase I |
C. maxima |
** |
|
EF062594 |
Cu-Zn SOD |
C. ficifolia |
** |
|
EF101660 EF101661 EF101662 EF101663 EF101664 EF101665 EF101666 EF101667 EF199760 EF199759 EF199758 EF199757 EF199756 EF199755 |
NBS resistance protein |
C. moschata |
** |
|
AB002695 |
aspartic endopeptidase |
C. pepo |
24 |
DHAR |
EF122791 |
dehydroascorbate reductase |
C. ficifolia |
** |
API |
DQ286449 DQ286448 DQ286447 DQ286445 DQ286444 DQ286443 DQ287856 |
aspartic acid proteinase inhibitor |
C. pepo C. maxima |
7 |
|
EF055184 EF055183 EF055180 |
16 kDa phloem protein 2 |
C. moschata C. ficifolia |
** |
PP16 |
DQ088368 DQ088369 DQ088370 DQ088371 DQ088372 DQ088373 |
16 kDa. phloem protein 2 |
C. maxima ‘Lefki kolokytha’ |
** |
PATL1 |
DQ251455 |
patellin 1 |
C. pepo ‘Fordhook’ |
49 |
|
E02079 |
glycerol-3-phosphate acyltransferase |
C. moschata |
** |
|
AJ628045 AJ630372 |
histidine kinase |
C. maxima |
** |
A215 |
X76086 |
14-3-3 protein endonuclease |
C. pepo |
43 |
EIN3 |
DQ023224 DQ023223 |
EIN3-like protein |
C. moschata |
** |
aprx |
Y17192 |
peroxidase |
C. pepo zucchini ‘Black Beauty’ |
** |
pfiAF4 |
X81647 |
fruit trypsin inhibitor |
C. maxima ‘Supermarket Hybrid’ |
** |
pfiBM7 |
X81447 |
chymotrypsin inhibitor |
C. maxima‘Supermarket Hybrid’ |
** |
|
X73314 |
Gibberellin 20-oxidase |
C. maxima‘Riesenm Elone, Gelb Genetzt’ |
** |
|
X55779 |
ascorbate oxidase |
Cucurbita spp. ‘Ebisu Nankin’ |
** |
pMCPN60-2 |
X70867 X70868 X68606 |
chaperonin 60 |
Cucurbita spp. ‘Kurokawa Amakuri’ |
** |
|
AJ829946 AJ829945 AJ829944 |
reverse transcriptase |
C. pepo |
** |
NIP1 |
AJ544830 |
Nod26-like protein |
C. pepo |
35 |
GAIP-B |
AY326307 AY326306 |
gibberellic acid insensitive phloem B |
C. maxima |
22 |
|
AY663852 |
serine/threonine kinase-like protein |
C. ficifolia |
** |
CPR |
AB116239 |
oxidosqualene cyclase |
C. pepo |
** |
CPQ |
AB116238 |
cucurbitadienol synthase |
C. pepo |
** |
|
AY672635 |
chymotrypsin protease inhibitor |
C. maxima |
** |
|
AY672634 |
aspartic protease inhibitor |
C. maxima |
** |
AIG-2 |
AY666083 |
aspartic protease inhibitor |
C. maxima |
** |
AIG-1 |
AY666082 |
aspartic protease inhibitor |
C. maxima |
** |
rpl2 |
AY396281 |
ribosomal protein L2 |
C. pepo |
12 |
rpl23 |
AY396396 |
ribosomal protein L23 |
C. pepo |
12 |
rps19 |
AY396376 |
ribosomal protein S19 |
C. pepo |
12 |
psbC |
AY396185 |
photosystem II protein |
C. pepo |
12 |
rpoB |
AY396320 |
polymerase beta subunit |
C. pepo |
12 |
rps2 |
AY396301 |
ribosomal protein S2 |
C. pepo |
12 |
FAD2 |
AY525163 |
omega-6 fatty acid desaturase |
C. pepo |
** |
matR |
AY453101 |
maturase |
C. pepo |
3 |
GAS1 |
AY379783 |
galactinol synthase |
C. pepo |
2 |
atpB |
AF209573 |
ATP synthase beta subunit |
C. pepo |
** |
Pugf |
AB059484 |
glutathione S-transferase |
C. maxima |
25 |
nad1 nad2 |
AF453584 through AF453645 |
NADH dehydrogenase subunit 1 and 2 |
C. pepo ssp. pepo C. pepo ssp. fraterna C. pepo ssp. ovifera C. pepo var. texana C. pepo var. ozarkana C. moschata C. maxima C. foetidissima C. argyrosperma C. sororia C. ecuadorensis C. andreana; C. okeechobeensis ssp. martinezii |
51 |
CmMP73 |
AB062669 |
preproMP73 |
C. maxima‘Kurokawa Amakuri Nankin’ |
** |
CmATS1;2 |
AB042401 AB042400 |
glycerol-3-phosphate acyltransferase |
C. moschata |
** |
|
AF260736 |
glucose-6-phosphate dehydrogenase |
C. pepo |
** |
|
AF260735 AF260734 AF260733 AF260732 |
NADP-dependent malic enzyme |
C. pepo |
** |
|
AF260731 |
heat shock protein 70 |
C. pepo |
** |
API-2 API-1 |
AF038167 AF038166 |
aspartic proteinase inhibitor |
C. maxima |
8 |
* Gene symbols were assigned by the researchers isolating the gene; they have no correspondence to the official Cucurbita gene symbols. **Unpublished: Genes can be submitted directly to Genbank, wthout being published in a journal. *** ‘Kurokawa Amakuri Nankin’ was identified only as “ Cucurbita sp.”
Literature Cited in Table 4
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