Maize germinal cell initials accommodate hypoxia and precociously express meiotic genes.

Maize germinal cell initials accommodate hypoxia and precociously express meiotic genes.
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DOI:
10.1111/tpj.12414
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发表时间:
2014-02
期刊:
The Plant journal : for cell and molecular biology
影响因子:
--
通讯作者:
Walbot V
Walbot V
中科院分区:
其他
文献类型:
--
作者:
Kelliher T;Walbot V

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In flowering plants, anthers are the site of de novo germinal cell specification, male meiosis, and pollen development. Atypically, anthers lack a meristem. Instead, both germinal and somatic cell types differentiate from floral stem cells packed into anther lobes. To better understand anther cell fate specification and to provide a resource for the reproductive biology community, we isolated cohorts of germinal and somatic initials from maize anthers within 36 hours of fate acquisition, identifying 815 specific and 1714 significantly enriched germinal transcripts, plus 2439 specific and 2112 significantly enriched somatic transcripts. To clarify transcripts involved in cell differentiation, we contrasted these profiles to anther primordia prior to fate specification and to msca1 anthers arrested in the first step of fate specification and hence lacking normal cell types. The refined cell-specific profiles demonstrate that both germinal and somatic cell populations differentiate quickly and express unique transcription factor sets; a subset of transcript localizations were validated by in situ hybridization. Surprisingly, germinal initials starting five days of mitotic divisions were significantly enriched in >100 transcripts classified in meiotic processes including recombination and synapsis, along with gene sets involved in RNA metabolism, redox homeostasis, and cytoplasmic ATP generation. Enrichment of meiotic-specific genes in germinal initials challenges current dogma that the mitotic to meiotic transition occurs later in development during pre-meiotic S phase. Expression of cytoplasmic energy generation genes suggests that male germinal cells accommodate hypoxia by diverting carbon away from mitochondrial respiration into alternative pathways that avoid producing reactive oxygen species (ROS).
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