4.6 Article

Biphasic regulation of the transcription factor ABORTED MICROSPORES (AMS) is essential for tapetum and pollen development in Arabidopsis

Journal

NEW PHYTOLOGIST
Volume 213, Issue 2, Pages 778-790

Publisher

WILEY
DOI: 10.1111/nph.14200

Keywords

aborted microspores (AMS); anther development; Arabidopsis thaliana; pollen development; regulatory network modelling; tapetum

Categories

Funding

  1. Biotechnology and Biological Sciences Research Council [BB/J001295/1]
  2. National Natural Science Foundation of China [31110103915]
  3. BBSRC [BB/J001295/1] Funding Source: UKRI
  4. Biotechnology and Biological Sciences Research Council [BB/J001295/1, BBS/OS/NW/000005] Funding Source: researchfish
  5. The British Council [GII107] Funding Source: researchfish

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Viable pollen is essential for plant reproduction and crop yield. Its production requires coordinated expression at specific stages during anther development, involving early meiosis-associated events and late pollen wall formation. The ABORTED MICROSPORES (AMS) transcription factor is a master regulator of sporopollenin biosynthesis, secretion and pollen wall formation in Arabidopsis. Here we show that it has complex regulation and additional essential roles earlier in pollen formation. An inducible-AMS reporter was created for functional rescue, protein expression pattern analysis, and to distinguish between direct and indirect targets. Mathematical modelling was used to create regulatory networks based on wild-type RNA and protein expression. Dual activity of AMS was defined by biphasic protein expression in anther tapetal cells, with an initial peak around pollen meiosis and then later during pollen wall development. Direct AMS-regulated targets exhibit temporal regulation, indicating that additional factors are associated with their regulation. We demonstrate that AMS biphasic expression is essential for pollen development, and defines distinct functional activities during early and late pollen development. Mathematical modelling suggests that AMS may competitively form a protein complex with other tapetum-expressed transcription factors, and that biphasic regulation is due to repression of upstream regulators and promotion of AMS protein degradation.

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