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拟南芥条件性光合作用突变体abc1k1和var2积累部分加工的类囊体前体蛋白,并且在叶绿体生物发生方面存在缺陷。

Arabidopsis conditional photosynthesis mutants abc1k1 and var2 accumulate partially processed thylakoid preproteins and are defective in chloroplast biogenesis.

作者信息

Collombat Joy, Quadroni Manfredo, Douet Véronique, Pipitone Rosa, Longoni Fiamma, Kessler Felix

机构信息

Institute of biology, Plant Physiology Laboratory, Université de Neuchâtel, 2000, Neuchâtel, Switzerland.

Protein Analysis Facility (PAF), Université de Lausanne, 1015, Lausanne, Switzerland.

出版信息

Commun Biol. 2025 Jan 22;8(1):111. doi: 10.1038/s42003-025-07497-y.

Abstract

Photosynthetic activity is established during chloroplast biogenesis. In this study we used 680 nm red light to overexcite Photosystem II and disrupt photosynthesis in two conditional mutants (var2 and abc1k1) which reversibly arrested chloroplast biogenesis. During biogenesis, chloroplasts import most proteins associated with photosynthesis. Some of these must be inserted in or transported across the thylakoid membrane into the thylakoid lumen. They are synthesized in the cytoplasm with cleavable targeting sequences and the lumenal ones have bi-partite targeting sequences (first for the chloroplast envelope, second for the thylakoid membrane). Cleavage of these peptides is required to establish photosynthesis and a critical step of chloroplast biogenesis. We employ a combination of Western blotting and mass spectrometry to analyze proteins in var2 and abc1k1. Under red light, var2 and abc1k1 accumulated incompletely cleaved processing intermediates of thylakoid proteins. These findings correlated with colorless cotyledons, and defects in both chloroplast morphology and photosynthesis. Together the results provide evidence for the requirement of active photosynthesis for processing of photosystem-associated thylakoid proteins and concomitantly progression of chloroplast biogenesis.

摘要

光合活性在叶绿体生物发生过程中得以确立。在本研究中,我们使用680纳米的红光过度激发光系统II,并破坏两个条件突变体(var2和abc1k1)的光合作用,这两个突变体会可逆地阻止叶绿体生物发生。在生物发生过程中,叶绿体导入大多数与光合作用相关的蛋白质。其中一些蛋白质必须插入类囊体膜或穿过类囊体膜进入类囊体腔。它们在细胞质中合成,带有可切割的靶向序列,而腔中的蛋白质具有双部分靶向序列(首先针对叶绿体包膜,其次针对类囊体膜)。这些肽的切割是建立光合作用所必需的,也是叶绿体生物发生的关键步骤。我们采用蛋白质免疫印迹法和质谱分析法相结合的方法来分析var2和abc1k1中的蛋白质。在红光下,var2和abc1k1积累了类囊体蛋白不完全切割的加工中间体。这些发现与无色子叶以及叶绿体形态和光合作用的缺陷相关。这些结果共同为光系统相关类囊体蛋白的加工以及叶绿体生物发生的进展需要活跃光合作用提供了证据。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f88e/11754785/66dfbb49d14b/42003_2025_7497_Fig1_HTML.jpg

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