The rice tapetum degeneration retardation gene is required for tapetum degradation and anther development

被引:624
作者
Li, Na
Zhang, Da-Sheng
Liu, Hai-Sheng
Yin, Chang-Song
Li, Xiao-xing
Liang, Wan-Qi
Yuan, Zheng
Xu, Ben
Chu, Huang-Wei
Wang, Jia
Wen, Tie-Qiao
Huang, Hai
Luo, Da
Ma, Hong
Zhang, Da-Bing [1 ]
机构
[1] Shanghai Jiao Tong Univ, Shanghai Inst Biol Sci,Minist Educ, Penn State Univ,Key Lab Microbial Metab, Joint Ctr Life Sci,Sch Life Sci & Biotechnol, Shanghai 200240, Peoples R China
[2] Shanghai Univ, Coll Life Sci, Shanghai 200436, Peoples R China
[3] Chinese Acad Sci, Shanghai Inst Biol Sci, Inst Plant Physiol & Ecol, Shanghai 200032, Peoples R China
[4] Penn State Univ, Dept Biol, Huck Inst Life Sci, University Pk, PA 16082 USA
关键词
D O I
10.1105/tpc.106.044107
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
In flowering plants, tapetum degeneration is proposed to be triggered by a programmed cell death (PCD) process during late stages of pollen development; the PCD is thought to provide cellular contents supporting pollen wall formation and to allow the subsequent pollen release. However, the molecular basis regulating tapetum PCD in plants remains poorly understood. We report the isolation and characterization of a rice (Oryza sativa) male sterile mutant tapetum degeneration retardation (tdr), which exhibits degeneration retardation of the tapetum and middle layer as well as collapse of microspores. The TDR gene is preferentially expressed in the tapetum and encodes a putative basic helix-loop-helix protein, which is likely localized to the nucleus. More importantly, two genes, Os CP1 and Os c6, encoding a Cys protease and a protease inhibitor, respectively, were shown to be the likely direct targets of TDR through chromatin immunoprecipitation analyses and the electrophoretic mobility shift assay. These results indicate that TDR is a key component of the molecular network regulating rice tapetum development and degeneration.
引用
收藏
页码:2999 / 3014
页数:16
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