Hida Shintaro, Nishio Marie, Uesaka Kazuma, Banba Mari, Takatani Nobuyuki, Yamamoto Haruki, Ihara Kunio, Fujita Yuichi
Graduate School of Bioagricultural Sciences, Nagoya University, Furo-cho, Chikusa-ku, Nagoya 464-8601, Japan.
Institute for Gene Research, Nagoya University, Furo-cho, Chikusa-ku, Nagoya 464-8602, Japan.
Plant Cell Physiol. 2025 Aug 12;66(7):1102-1118. doi: 10.1093/pcp/pcaf043.
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.
寄生植物的普遍存在表明在自然环境中光合能力丧失的现象频繁发生进化。然而,尚无研究观察到光合能力丧失这样的进化事件。在此,我们报告了一些突变,这些突变导致蓝细菌博氏纤细席藻暗适应变体的光合生长能力丧失或降低,该变体即使在黑暗中也能进行异养生长。我们通过在含有葡萄糖的琼脂平板上培养博氏纤细席藻分离出了28个暗适应变体,并通过每10 - 14天接种一次,在暗异养条件下将它们维持7 - 49个月。所有变体的暗异养生长均显著快于亲本菌株,其中15个变体同时丧失了光合生长能力。基因组重测序显示,28个变体中有19个在一个编码PP2C型丝氨酸磷酸酶的共同单基因(LBWT_21500)中携带了各种突变。对LBWT_21500基因敲除突变体的表征表明,LBWT_21500的缺失导致了暗异养生长加快与光合生长减慢之间的权衡,这表明LBWT_21500中的突变导致了19个变体中8个变体的表型,而其他额外的突变导致了另外11个变体光合生长能力的丧失。转录组分析表明,该磷酸酶参与了全局转录调控系统,该系统利用伴侣切换系统的模块优化光合和暗异养代谢。我们提议将LBWT_21500命名为光养 - 异养转换磷酸酶。全局转录调控系统中的突变可能是导致光合能力丧失的进化步骤之一。