| Literature DB >> 32391618 |
Lijun Ren1,2, Tingting Zhao1,2, Lei Zhang3, Guijie Du1, Yi Shen1, Ding Tang1, Yafei Li1, Qiong Luo4, Zhukuan Cheng1,2.
Abstract
Highly coordinated pollen wall patterning is essential for male reproductive development. Here, we report the identification of Defective Microspore Development 1 (DMD1), which encodes a nuclear-localized protein possessing transactivation activity. DMD1 is preferentially expressed in the tapetum and microspores during post-meiotic development. Mutations in DMD1 cause a male-sterile phenotype with impaired microspore cell integrity. The mutants display abnormal callose degradation, accompanied by inhibited primexine thickening in the newly released microspores. Several genes associated with callose degradation and primexine formation are downregulated in dmd1 anthers. In addition, irregular Ubisch body morphology and discontinuous endexine occur, and the baculum is completely absent in dmd1. DMD1 interacts with Tapetum Degeneration Retardation (TDR), a basic helix-loop-helix transcription factor required for exine formation. Taken together, our results suggest that DMD1 is responsible for microspore cell integrity, primexine formation and exine pattern formation during Oryza sativa (rice) microspore development.Entities:
Keywords: male sterility; microspore; pollen; primexine; rice
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Year: 2020 PMID: 32391618 DOI: 10.1111/tpj.14811
Source DB: PubMed Journal: Plant J ISSN: 0960-7412 Impact factor: 6.417