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陆地殖民可能是植物中线粒体逆行信号进化的驱动力。

The colonization of land was a likely driving force for the evolution of mitochondrial retrograde signalling in plants.

机构信息

Department of Biology, Lund University, Lund, Sweden.

出版信息

J Exp Bot. 2022 Nov 19;73(21):7182-7197. doi: 10.1093/jxb/erac351.

DOI:10.1093/jxb/erac351
PMID:36055768
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9675596/
Abstract

Most retrograde signalling research in plants was performed using Arabidopsis, so an evolutionary perspective on mitochondrial retrograde regulation (MRR) is largely missing. Here, we used phylogenetics to track the evolutionary origins of factors involved in plant MRR. In all cases, the gene families can be traced to ancestral green algae or earlier. However, the specific subfamilies containing factors involved in plant MRR in many cases arose during the transition to land. NAC transcription factors with C-terminal transmembrane domains, as observed in the key regulator ANAC017, can first be observed in non-vascular mosses, and close homologs to ANAC017 can be found in seed plants. Cyclin-dependent kinases (CDKs) are common to eukaryotes, but E-type CDKs that control MRR also diverged in conjunction with plant colonization of land. AtWRKY15 can be traced to the earliest land plants, while AtWRKY40 only arose in angiosperms and AtWRKY63 even more recently in Brassicaceae. Apetala 2 (AP2) transcription factors are traceable to algae, but the ABI4 type again only appeared in seed plants. This strongly suggests that the transition to land was a major driver for developing plant MRR pathways, while additional fine-tuning events have appeared in seed plants or later. Finally, we discuss how MRR may have contributed to meeting the specific challenges that early land plants faced during terrestrialization.

摘要

大多数植物的逆行信号研究都是使用拟南芥进行的,因此,线粒体逆行调节(MRR)的进化视角在很大程度上是缺失的。在这里,我们使用系统发生学来追踪参与植物 MRR 的因素的进化起源。在所有情况下,这些基因家族都可以追溯到祖先的绿藻或更早的时期。然而,在许多情况下,参与植物 MRR 的特定亚家族在向陆地过渡时产生。具有 C 端跨膜结构域的 NAC 转录因子,如关键调节因子 ANAC017 中观察到的,首先可以在非维管束苔藓中观察到,并且与 ANAC017 密切同源的因子可以在种子植物中找到。细胞周期蛋白依赖性激酶(CDKs)是真核生物所共有的,但控制 MRR 的 E 型 CDK 也与植物登陆陆地一起分化。AtWRKY15 可以追溯到最早的陆地植物,而 AtWRKY40 仅在被子植物中出现,AtWRKY63 甚至在最近的十字花科植物中出现。AP2 转录因子可追溯到藻类,但 ABI4 型再次仅出现在种子植物中。这强烈表明,向陆地的过渡是开发植物 MRR 途径的主要驱动力,而在种子植物或更晚的时期出现了其他微调事件。最后,我们讨论了 MRR 如何有助于应对早期陆地植物在陆地化过程中面临的特定挑战。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/44e3/9675596/08d881e33782/erac351f0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/44e3/9675596/d8f780646575/erac351f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/44e3/9675596/a61d66796da3/erac351f0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/44e3/9675596/dccebc0897e3/erac351f0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/44e3/9675596/08d881e33782/erac351f0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/44e3/9675596/d8f780646575/erac351f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/44e3/9675596/a61d66796da3/erac351f0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/44e3/9675596/dccebc0897e3/erac351f0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/44e3/9675596/08d881e33782/erac351f0004.jpg

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