Center for Photosynthesis and Plant Stress Biology, College of Life Sciences, South-China Agricultural University, Guangzhou, 510642, China.
State Key Laboratory for Conservation and Utilization of Subtropical Agro-Bioresources, College of Life Sciences, South China Agricultural University, Guangzhou, 510642, China.
Plant Cell Rep. 2024 Nov 23;43(12):292. doi: 10.1007/s00299-024-03376-8.
Through the study of a point mutation of AtECB2, it is reconfirmed that AtECB2 plays an important role in the early development of chloroplast. AtECB2(EARLY CHLOROPLAST BIOGENESIS 2, At1g15510), a member of the pentatricopeptide repeat motif proteins (PPR) superfamily, and its loss of function mutation ecb2-1causes seedling lethal, while a point mutation ecb2-2 causes delayed chloroplast development. Finding more AtECB2 weak alleles helps to understand the molecular mechanisms of AtECB2. In this study, a leaf virescence mutant was identified from ethylmethane sulfonate (EMS) treated Arabidopsis Col-0 M2 mutants library. The mutation of this mutant was first confirmed as a recessive mutation of one gene through the phenotype of F1 and its F2 phenotype segregation of this mutant crossed with Col-0. The mutation of G1931A of AtECB2 is identified as the cause of this leaf virescence phenotype sequentially through positional cloning, whole genome resequencing, Sanger sequencing and complementation. Therefore, we named this weak allele of AtECB2 as ecb2-3. The chlorophyll content and photosystem II maximum photochemical efficiency of ecb2-3 are obviously lower than that of Col-0 and its complementation lines, respectively. The chloroplast development of ecb2-3 is also inferior to that of Col-0 and its complementation line at the observed time points using the transmission electron microscope. The RNA editing efficiency of three chloroplast gene sites (accD C794 and C1568, ndhF C290) was observed much lower compared with that of Col-0 and its complementation line. In summary, AtECB2 plays an important role in early chloroplast biogenesis through related chloroplast gene editing regulation, and this weak mutant ecb2-3 may be useful material in dissecting the function of AtECB2 in the near future.
通过对 AtECB2 的一个点突变的研究,再次证实了 AtECB2 在叶绿体的早期发育中起着重要作用。AtECB2(EARLY CHLOROPLAST BIOGENESIS 2,At1g15510)是五肽重复基序蛋白(PPR)超家族的成员,其功能丧失突变 ecb2-1 导致幼苗致死,而点突变 ecb2-2 导致叶绿体发育延迟。发现更多的 AtECB2 弱等位基因有助于理解 AtECB2 的分子机制。在本研究中,从乙基甲磺酸(EMS)处理的拟南芥 Col-0 M2 突变体文库中鉴定出一个叶片黄化突变体。通过该突变体与 Col-0 杂交的 F1 及其 F2 表型分离,首先确认该突变是一个基因的隐性突变。通过定位克隆、全基因组重测序、Sanger 测序和互补实验,依次鉴定出 AtECB2 的 G1931A 突变是导致该叶片黄化表型的原因。因此,我们将该 AtECB2 的弱等位基因命名为 ecb2-3。ecb2-3 的叶绿素含量和光系统 II 最大光化学效率明显低于 Col-0 和其互补系,在用透射电子显微镜观察时,ecb2-3 的叶绿体发育也劣于 Col-0 和其互补系。与 Col-0 和其互补系相比,三个叶绿体基因位点(accD C794 和 C1568、ndhF C290)的 RNA 编辑效率明显较低。综上所述,AtECB2 通过相关的叶绿体基因编辑调控在叶绿体的早期生物发生中起着重要作用,这个弱突变体 ecb2-3 可能在不久的将来成为解析 AtECB2 功能的有用材料。