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本文引用的文献

1
A maize glutaredoxin gene, abphyl2, regulates shoot meristem size and phyllotaxy.一个玉米谷氧还蛋白基因abphyl2调控茎尖分生组织大小和叶序。
Plant Cell. 2015 Jan;27(1):121-31. doi: 10.1105/tpc.114.130393. Epub 2015 Jan 23.
2
A regulatory framework for shoot stem cell control integrating metabolic, transcriptional, and phytohormone signals.调控茎尖干细胞的代谢、转录和植物激素信号整合的调控框架。
Dev Cell. 2014 Feb 24;28(4):438-49. doi: 10.1016/j.devcel.2014.01.013.
3
The ERECTA receptor kinase regulates Arabidopsis shoot apical meristem size, phyllotaxy and floral meristem identity.ERECTA 受体激酶调控拟南芥茎尖分生组织大小、叶序和花分生组织身份。
Development. 2014 Feb;141(4):830-41. doi: 10.1242/dev.104687.
4
Regulatory modules controlling maize inflorescence architecture.调控玉米花序结构的调控模块。
Genome Res. 2014 Mar;24(3):431-43. doi: 10.1101/gr.166397.113. Epub 2013 Dec 4.
5
Unequal redundancy in maize knotted1 homeobox genes.玉米knotted1同源异型框基因中的不等冗余
Plant Physiol. 2014 Jan;164(1):229-38. doi: 10.1104/pp.113.228791. Epub 2013 Nov 11.
6
The maize Gα gene COMPACT PLANT2 functions in CLAVATA signalling to control shoot meristem size.玉米 Gα 基因 COMPACT PLANT2 在 CLAVATA 信号途径中起作用,控制茎分生组织的大小。
Nature. 2013 Oct 24;502(7472):555-8. doi: 10.1038/nature12583. Epub 2013 Sep 11.
7
ERECTA family genes regulate auxin transport in the shoot apical meristem and forming leaf primordia.ERECTA 家族基因调节茎尖分生组织中的生长素运输和形成叶原基。
Plant Physiol. 2013 Aug;162(4):1978-91. doi: 10.1104/pp.113.218198. Epub 2013 Jul 2.
8
Plant stem cell maintenance involves direct transcriptional repression of differentiation program.植物干细胞的维持涉及分化程序的直接转录抑制。
Mol Syst Biol. 2013;9:654. doi: 10.1038/msb.2013.8.
9
Grass meristems I: shoot apical meristem maintenance, axillary meristem determinacy and the floral transition.草茎分生组织 I:茎尖分生组织的维持、腋芽分生组织的确定性和花的转变。
Plant Cell Physiol. 2013 Mar;54(3):302-12. doi: 10.1093/pcp/pct025. Epub 2013 Feb 14.
10
Quantitative variation in maize kernel row number is controlled by the FASCIATED EAR2 locus.玉米穗行数的数量变化受 FASCIATED EAR2 基因座控制。
Nat Genet. 2013 Mar;45(3):334-7. doi: 10.1038/ng.2534. Epub 2013 Feb 3.

簇生穗4编码一种bZIP转录因子,该因子调控玉米茎尖分生组织的大小。

FASCIATED EAR4 encodes a bZIP transcription factor that regulates shoot meristem size in maize.

作者信息

Pautler Michael, Eveland Andrea L, LaRue Therese, Yang Fang, Weeks Rebecca, Lunde China, Je Byoung Il, Meeley Robert, Komatsu Mai, Vollbrecht Erik, Sakai Hajime, Jackson David

机构信息

Cold Spring Harbor Laboratory, Cold Spring Harbor, New York 11724.

Department of Genetics, Development, and Cell Biology, Iowa State University, Ames, Iowa 50010.

出版信息

Plant Cell. 2015 Jan;27(1):104-20. doi: 10.1105/tpc.114.132506. Epub 2015 Jan 23.

DOI:10.1105/tpc.114.132506
PMID:25616871
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4330574/
Abstract

Plant architecture is dictated by precise control of meristematic activity. In the shoot, an imbalance in positive or negative maintenance signals can result in a fasciated or enlarged meristem phenotype. fasciated ear4 (fea4) is a semidwarfed mutant with fasciated ears and tassels as well as greatly enlarged vegetative and inflorescence meristems. We identified FEA4 as a bZIP transcription factor, orthologous to Arabidopsis thaliana PERIANTHIA. FEA4 was expressed in the peripheral zone of the vegetative shoot apical meristem and in the vasculature of immature leaves and conspicuously excluded from the stem cell niche at the tip of the shoot apical meristem and from incipient leaf primordia. Following the transition to reproductive fate, FEA4 was expressed throughout the entire inflorescence and floral meristems. Native expression of a functional YFP:FEA4 fusion recapitulated this pattern of expression. We used chromatin immunoprecipitation-sequencing to identify 4060 genes proximal to FEA4 binding sites, including ones that were potentially bound and modulated by FEA4 based on transcriptional changes in fea4 mutant ears. Our results suggest that FEA4 promotes differentiation in the meristem periphery by regulating auxin-based responses and genes associated with leaf differentiation and polarity, potentially in opposition to factors such as KNOTTED1 and WUSCHEL.

摘要

植物结构由分生组织活性的精确控制所决定。在茎尖,正向或负向维持信号的失衡会导致分生组织出现扁化或增大的表型。扁化穗4(fea4)是一个半矮化突变体,其穗和雄穗扁化,营养分生组织和花序分生组织也大幅增大。我们将FEA4鉴定为一种bZIP转录因子,与拟南芥的PERIANTHIA直系同源。FEA4在营养茎尖分生组织的外周区以及未成熟叶片的维管系统中表达,明显排除在茎尖分生组织顶端的干细胞龛和初始叶原基之外。在转变为生殖命运后,FEA4在整个花序和花分生组织中表达。功能性YFP:FEA4融合蛋白的天然表达重现了这种表达模式。我们使用染色质免疫沉淀测序来鉴定FEA4结合位点附近的4060个基因,包括基于fea4突变穗中的转录变化而可能被FEA4结合和调控的基因。我们的结果表明,FEA4通过调节基于生长素的反应以及与叶分化和极性相关的基因,促进分生组织外周的分化,这可能与诸如KNOTTED1和WUSCHEL等因子相反。