Location: Corn Insects and Crop Genetics Research
Title: Sequence, assembly and annotation of maize inbred B104Author
MANCHANDA, NANCY - Iowa State University | |
CHOUGULE, KAPEEL - Cold Spring Harbor Laboratory | |
OLSON, ANDREW - Cold Spring Harbor Laboratory | |
FENGLER, KEVIN - Corteva Agriscience | |
SEETHARAM, ARUN - Iowa State University | |
LIACA, VICTOR - Corteva Agriscience | |
ZASTROW-HAYES, GINA - Corteva Agriscience | |
WEI, SHARON - Cold Spring Harbor Laboratory | |
BRAUN, IAN - Iowa State University | |
Lopez, Miriam | |
PLOYARAM, WIRIYANAT - Iowa State University | |
ZARECOR, SCOTT - Iowa State University | |
LU, ZEFU - University Of Georgia | |
WALLEY, JUSTIN - Iowa State University | |
YANDEAU-NELSON, MARNA - Iowa State University | |
WANG, KAN - Iowa State University | |
ADAMS, DEAN - Iowa State University | |
Ware, Doreen | |
SCHMITZ, BOB - University Of Georgia | |
Woodhouse, Margaret | |
Lauter, Nicholas | |
Andorf, Carson | |
LAWRENCE-DILL, CAROLYN - Iowa State University | |
HUFFORD, MATTHEW - Iowa State University |
Submitted to: Maize Annual Meetings
Publication Type: Abstract Only Publication Acceptance Date: 3/6/2021 Publication Date: 3/8/2021 Citation: Manchanda, N., Chougule, K., Olson, A., Fengler, K., Seetharam, A., Liaca, V., Zastrow-Hayes, G., Wei, S., Braun, I., Lopez, M.D., Ployaram, W., Zarecor, S., Lu, Z., Walley, J., Yandeau-Nelson, M., Wang, K., Adams, D., Ware, D., Schmitz, B., Woodhouse, M.H., Lauter, N.C., Andorf, C.M., Lawrence-Dill, C., Hufford, M. 2021. Sequence, assembly and annotation of maize inbred B104. Maize Annual Meetings. 76. Interpretive Summary: Technical Abstract: B104 is a highly transformable maize inbred line which shows high sequence similarity with the reference maize line B73. B73 and B104 inbred lines share the same background; they were developed as part of the Iowa Stiff Stalk Synthetic breeding program. To understand the dynamics and tempo of maize genome evolution within a modern maize breeding program and enhance our knowledge of maize transformation, we have generated a high-quality genome assembly of B104. The new assembly was generated using high-depth PacBio data and a Bionano optical map and is significantly more contiguous and complete (32 scaffolds and 98Mb N50) than the previous draft assembly based on short-read data. RNA-seq from multiple tissues was used to annotate the assembly using an evidence-driven and ab-initio approach. Transposable Elements (TEs) were annotated in the B104 genome using a pipeline that combines homology based-annotations with the structure-based annotations to provide a complete summary of the transposons. We characterized both large-scale (>1Mb) and small- to medium- scale (50bp - 1Mb) structural variations using read and genome alignment based approaches. To characterize the differences in the contributions of stiffstalk founder lines to B73 and B104 and explore how this governs patterns of structural variation, transposon, and methylation variation, we painted the genomes with the founder haplotypes and identified regions of shared and distinct founder ancestry. We explored the gene content variation between B73 and B104, based on the complete set of structural annotations from B104, B73 and 25 NAM founder lines and identified the number of core (50%), dispensable (44.6%) and private genes (5%) in B104. We further identified genes which are differentially expressed (1.3%) between B73 and B104 across the 10 tissues. We present a summary of structural variations including genic presence/absence, variation in gene expression and TE families across regions of shared and different founder ancestry. |