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自噬调控拟南芥雄性配子体育性并控制肌动蛋白的组织。

Autophagy modulates Arabidopsis male gametophyte fertility and controls actin organization.

机构信息

College of Life Sciences, South China Agricultural University, Guangzhou, China.

School of Biology and Agriculture, Shaoguan University, Shaoguan, China.

出版信息

Nat Commun. 2024 Nov 21;15(1):10071. doi: 10.1038/s41467-024-54468-8.

DOI:10.1038/s41467-024-54468-8
PMID:39567510
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11579482/
Abstract

Autophagy, a crucial mechanism for cellular degradation, is regulated by conserved autophagy-related (ATG) core proteins across species. Impairments in autophagy result in significant developmental and reproductive aberrations in mammals. However, autophagy is thought to be functionally dispensable in Arabidopsis thaliana since most of the ATG mutants lack severe growth and reproductive defects. Here, we challenge this perception by unveiling a role for autophagy in male gametophyte development and fertility in Arabidopsis. A detailed re-assessment of atg5 and atg7 mutants found that reduced autophagy activity in germinated pollen accompanied by partial aberrations in sperm cell biogenesis and pollen tube growth, leading to compromised seed formation. Furthermore, we revealed autophagy modulates the spatial organization of actin filaments via targeted degradation of actin depolymerization factors ADF7 and Profilin2 in pollen grains and tubes through a key receptor, Neighbor of BRCA1 (NBR1). Our findings advance the understanding of the evolutionary conservation and diversification of autophagy in modulating male fertility in plants contrasting to mammals.

摘要

自噬作用是一种细胞降解的关键机制,在不同物种中由保守的自噬相关(ATG)核心蛋白来调节。自噬作用的损伤会导致哺乳动物出现显著的发育和生殖异常。然而,自噬作用在拟南芥中被认为是可有可无的,因为大多数 ATG 突变体缺乏严重的生长和生殖缺陷。在这里,我们通过揭示自噬作用在拟南芥雄性配子体发育和育性中的作用来挑战这一观点。对 atg5 和 atg7 突变体的详细重新评估发现,萌发花粉中的自噬活性降低,伴随着精子细胞发生和花粉管生长的部分异常,导致种子形成受损。此外,我们揭示了自噬作用通过靶向降解花粉粒和花粉管中的肌动蛋白解聚因子 ADF7 和 Profilin2 来调节肌动蛋白丝的空间组织,通过一个关键受体 Neighbor of BRCA1 (NBR1)。我们的发现推进了对自噬作用在调节植物雄性育性方面的进化保守性和多样化的理解,与哺乳动物形成对比。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1604/11579482/282d16fd070f/41467_2024_54468_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1604/11579482/4f2169ca836b/41467_2024_54468_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1604/11579482/6dd2c7cd9851/41467_2024_54468_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1604/11579482/926fa5905e08/41467_2024_54468_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1604/11579482/fa8934ce47ce/41467_2024_54468_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1604/11579482/6919f41213a7/41467_2024_54468_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1604/11579482/282d16fd070f/41467_2024_54468_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1604/11579482/4f2169ca836b/41467_2024_54468_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1604/11579482/6dd2c7cd9851/41467_2024_54468_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1604/11579482/926fa5905e08/41467_2024_54468_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1604/11579482/fa8934ce47ce/41467_2024_54468_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1604/11579482/6919f41213a7/41467_2024_54468_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1604/11579482/282d16fd070f/41467_2024_54468_Fig6_HTML.jpg

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