对暗适应变异体的基因组分析确定了磷酸酶基因phsP参与调节boryana蓝细菌的光合作用和暗异养生长。

IF 4 2区 生物学 Q2 CELL BIOLOGY
Shintaro Hida, Marie Nishio, Kazuma Uesaka, Mari Banba, Nobuyuki Takatani, Haruki Yamamoto, Kunio Ihara, Yuichi Fujita
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引用次数: 0

摘要

寄生植物的普遍存在表明在自然环境中光合能力丧失的频繁进化。然而,没有研究观察到像光合能力丧失这样的进化事件。在此,我们报道了导致黑暗适应蓝细菌瘦多利亚硼酸盐变种光合生长能力丧失或降低的突变,这种变体即使在黑暗中也能异养生长。在含葡萄糖的琼脂培养基上培养boryana Lejeunea,分离出28个黑暗适应变异,每10-14天接种一次,在黑暗异养条件下维持7-49个月。所有变异均表现出比亲本更快的暗异养生长,其中15个变异的光合生长能力下降。基因组重测序显示,28个变异中有19个在编码pp2c型丝氨酸磷酸酶的共同单基因(LBWT_21 500)中携带各种突变。LBWT_21 500敲除突变体的特征表明,LBWT_21 500的缺失导致了更快的暗异养生长和更慢的光合生长之间的权衡,这表明LBWT_21 500的突变导致了19个变体中8个的表型,而其他额外的突变导致了其他11个变体的光合生长能力丧失。转录组学分析表明,该磷酸酶参与了全球转录调控系统,该系统利用伴侣转换系统的模块优化光合作用和暗异养代谢。我们建议将LBWT_21 500命名为phsP(光养-异养转换磷酸酶)。全球转录调控系统的突变可能是导致光合能力丧失的进化步骤之一。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Genome analysis of dark-adapted variants identifies the phosphatase gene phsP involved in the regulation of photosynthetic and dark-heterotrophic growth in the cyanobacterium Leptolyngbya boryana.

The prevalence of parasitic plants suggests frequent evolution of photosynthetic capacity loss in the natural environments. However, no studies have observed such evolutionary events as the loss of photosynthetic capacity. Herein, we report mutations that lead to loss or decrease in the photosynthetic growth capacity of dark-adapted variants of the cyanobacterium Leptolyngbya boryana, which can grow heterotrophically even in the dark. We isolated 28 dark-adapted variants by culturing L. boryana on agar plates containing glucose and maintained them under dark-heterotrophic conditions for 7-49 months by inoculating every 10-14 days. All variants showed significantly faster dark-heterotrophic growth than the parental strains, accompanied by the loss of photosynthetic growth capacity in 15 variants. Genome resequencing revealed that 19 of the 28 variants carried various mutations in a common single gene (LBWT_21500) encoding PP2C-type serine phosphatase. Characterization of an LBWT_21500 knockout mutant revealed that the deletion of LBWT_21500 caused a trade-off between faster dark-heterotrophic growth and slower photosynthetic growth, suggesting that the mutations in LBWT_21500 are responsible for the phenotype of 8 of the 19 variants, while other additional mutations caused the loss of photosynthetic growth capacity in the other 11 variants. Transcriptomic analysis suggested that the phosphatase is involved in the global transcriptional regulatory system that optimizes photosynthetic and dark-heterotrophic metabolism using modules of the partner switching system. We proposed the name LBWT_21500 as phototrophic-heterotrophic switching phosphatase. Mutations in global transcriptional regulatory systems may serve as one of the evolutionary steps leading to the loss of photosynthetic capacity.

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来源期刊
Plant and Cell Physiology
Plant and Cell Physiology 生物-细胞生物学
CiteScore
8.40
自引率
4.10%
发文量
166
审稿时长
1.7 months
期刊介绍: Plant & Cell Physiology (PCP) was established in 1959 and is the official journal of the Japanese Society of Plant Physiologists (JSPP). The title reflects the journal''s original interest and scope to encompass research not just at the whole-organism level but also at the cellular and subcellular levels. Amongst the broad range of topics covered by this international journal, readers will find the very best original research on plant physiology, biochemistry, cell biology, molecular genetics, epigenetics, biotechnology, bioinformatics and –omics; as well as how plants respond to and interact with their environment (abiotic and biotic factors), and the biology of photosynthetic microorganisms.
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