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ARS Home » Midwest Area » Madison, Wisconsin » U.S. Dairy Forage Research Center » Research » Publications at this Location » Publication #183780
Title: GENETICS OF THE DST-MEDIATED MRNA DECAY PATHWAY USING A TRANSGENE BASED SELECTION

Author
item LIDDER, PREET - DELAWARE BIOTECHNOLOGY IN
item JOHNSON, MARK - HOWARD HUGHES MEDICAL
item Sullivan, Michael
item THOMPSON, DEBORAH - SANGER INSTITUTE, WELLCOM
item PEREZ-AMADOR, MIGUEL - INSTITUTO DE BIOLOGIA
item HOWARD, CHRISTIE - DEPT. OF BIOLOGY, UNIVERS
item GREEN, PAMELA - DELAWARE BIOTECHNOLOGY IN

Submitted to: Biochemical Society Transactions
Publication Type: Proceedings
Publication Acceptance Date: 3/20/2004
Publication Date: 8/1/2004
Citation: Lidder, P., Johnson, M.A., Sullivan, M.L., Thompson, D.M., Perez- Amador, M.A., Howard, C.J., Green, P.J. 2004. Genetics of the DST- mediated mRNA decay pathway using a transgene based selection. Biochemical Society Transactions. 32:575-577.

Interpretive Summary:

Technical Abstract: mRNA sequences that control abundance, localization and translation initiation have been identified, yet the factors that recognize these sequences are largely unknown. In this report, a transgene-based strategy designed to isolate mutants of rabidopsis thaliana that fail to recognize these sequences is described. In this strategy, a selectable gene and a screenable marker gene are put under the control of the sequence element being analysed and mutants are selected with altered abundance of the corresponding marker RNAs. The selection of mutants deficient in recognition of the DST (downstream) mRNA degradation signal is used as a test-case to illustrate some of the technical aspects that have facilitated success. Using this strategy, we report the isolation of a newmutant, dst3, deficient in the DST-mediatedmRNA decay pathway. The targeted genetic strategy described circumvents certain technical limitations of biochemical approaches. Hence, it provides a means to investigate a variety of other mechanisms responsible for post-transcriptional regulation.