Global gene expression analysis of the shoot apical meristem of maize (Zea mays L.)

被引:105
作者
Ohtsu, Kazuhiro
Smith, Marianne B.
Emrich, Scott J.
Borsuk, Lisa A.
Zhou, Ruilian
Chen, Tianle
Zhang, Xiaolan
Timmermans, Marja C. P.
Beck, Jon
Buckner, Brent
Janick-Buckner, Diane
Nettleton, Dan
Scanlon, Michael J.
Schnable, Patrick S. [1 ]
机构
[1] Iowa State Univ, Dept Agron, Ames, IA 50011 USA
[2] Iowa State Univ, Bioinformat & Comp Biol Grad Program, Ames, IA 50011 USA
[3] Univ Georgia, Dept Plant Biol, Athens, GA 30602 USA
[4] Cold Spring Harbor Lab, Cold Spring Harbor, NY 11724 USA
[5] Truman State Univ, Div Math & Comp Sci, Kirksville, MO 63501 USA
[6] Truman State Univ, Div Sci, Kirksville, MO 63501 USA
[7] Iowa State Univ, Dept Stat, Ames, IA 50011 USA
[8] Iowa State Univ, Ctr Plant Genom, Ames, IA 50011 USA
[9] Cornell Univ, Dept Plant Biol, Ithaca, NY 14853 USA
关键词
shoot apical meristem; global gene expression; laser capture microdissection; 454; sequencing; development; retrotransposon expression;
D O I
10.1111/j.1365-313X.2007.03244.x
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
All above-ground plant organs are derived from shoot apical meristems (SAMs). Global analyses of gene expression were conducted on maize (Zea mays L.) SAMs to identify genes preferentially expressed in the SAM. The SAMs were collected from 14-day-old B73 seedlings via laser capture microdissection (LCM). The RNA samples extracted from LCM-collected SAMs and from seedlings were hybridized to microarrays spotted with 37 660 maize cDNAs. Approximately 30% (10 816) of these cDNAs were prepared as part of this study from manually dissected B73 maize apices. Over 5000 expressed sequence tags (ESTs) (about 13% of the total) were differentially expressed (P < 0.0001) between SAMs and seedlings. Of these, 2783 and 2248 ESTs were up- and down-regulated in the SAM, respectively. The expression in the SAM of several of the differentially expressed ESTs was validated via quantitative RT-PCR and/or in situ hybridization. The up-regulated ESTs included many regulatory genes including transcription factors, chromatin remodeling factors and components of the gene-silencing machinery, as well as about 900 genes with unknown functions. Surprisingly, transcripts that hybridized to 62 retrotransposon-related cDNAs were also substantially up-regulated in the SAM. Complementary DNAs derived from the LCM-collected SAMs were sequenced to identify additional genes that are expressed in the SAM. This generated around 550 000 ESTs (454-SAM ESTs) from two genotypes. Consistent with the microarray results, approximately 14% of the 454-SAM ESTs from B73 were retrotransposon-related. Possible roles of genes that are preferentially expressed in the SAM are discussed.
引用
收藏
页码:391 / 404
页数:14
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