The ABORTED MICROSPORES Regulatory Network Is Required for Postmeiotic Male Reproductive Development in Arabidopsis thaliana

被引:294
作者
Xu, Jie [1 ]
Yang, Caiyun [2 ]
Yuan, Zheng [1 ,2 ]
Zhang, Dasheng [1 ]
Gondwe, Martha Y. [2 ]
Ding, Zhiwen [1 ]
Liang, Wanqi [1 ]
Zhang, Dabing [1 ,3 ]
Wilson, Zoe A. [2 ]
机构
[1] Shanghai Jiao Tong Univ, Sch Life Sci & Biotechnol, Shanghai 200240, Peoples R China
[2] Univ Nottingham, Sch Biosci, Loughborough LE12 5RD, Leics, England
[3] Shanghai Jiao Tong Univ, BioX Res Ctr, Minist Educ, Shanghai 200240, Peoples R China
基金
中国国家自然科学基金; 中国博士后科学基金;
关键词
PROGRAMMED-CELL-DEATH; TAPETUM-DEGENERATION-RETARDATION; TRANSCRIPTION FACTOR FAMILY; POLLEN WALL DEVELOPMENT; ACYL-COA SYNTHETASE; DNA-BINDING; DOMAIN PROTEIN; GENOME-WIDE; GENE ENCODES; SPOROPOLLENIN SYNTHESIS;
D O I
10.1105/tpc.109.071803
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The Arabidopsis thaliana ABORTED MICROSPORES (AMS) gene encodes a basic helix-loop-helix (bHLH) transcription factor that is required for tapetal cell development and postmeiotic microspore formation. However, the regulatory role of AMS in anther and pollen development has not been fully defined. Here, we show by microarray analysis that the expression of 549 anther-expressed genes was altered in ams buds and that these genes are associated with tapetal function and pollen wall formation. We demonstrate that AMS has the ability to bind in vitro to DNA containing a 6-bp consensus motif, CANNTG. Moreover, 13 genes involved in transportation of lipids, oligopeptides, and ions, fatty acid synthesis and metabolism, flavonol accumulation, substrate oxidation, methyl-modification, and pectin dynamics were identified as direct targets of AMS by chromatin immunoprecipitation. The functional importance of the AMS regulatory pathway was further demonstrated by analysis of an insertional mutant of one of these downstream AMS targets, an ABC transporter, White-Brown Complex homolog, which fails to undergo pollen development and is male sterile. Yeast two-hybrid screens and pulldown assays revealed that AMS has the ability to interact with two bHLH proteins (AtbHLH089 and AtbHLH091) and the ATA20 protein. These results provide insight into the regulatory role of the AMS network during anther development.
引用
收藏
页码:91 / 107
页数:17
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