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📅 2026-05-16
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Journal of integrative plant biology 2026-05-14
相关性 45/100

Uncovering the role of the PPR protein PHOTOSYSTEM ONE BIOGENESIS FACTOR6 in splicing chloroplast group II introns.

揭示PPR蛋白PBF6在剪接叶绿体II型内含子中的作用

Li M, Sun M, Lv J, Song M, Lu S, Zhang A, Lu C

酶/系统类型: RNase III(RNC1)作为多亚基剪接复合体组分参与叶绿体II型内含子剪接
机制要点: PBF6通过其N端10个PPR基序特异性结合ycf3内含子1、clpP1内含子2以及petB、ndhA、ndhB转录本的内含子,并招募CRM、肽酰-tRNA水解酶、RNase III(RNC1)、PORR、APO、DEAD-box RNA解旋酶和mTERF家族等已知剪接因子,形成约600 kDa和约300 kDa的两个多亚基剪接复合体,分别包含9个和3个已知剪接因子,从而促进内含子剪接。
工程化与应用: 未涉及蛋白优化、突变设计或底物特异性重编程;但揭示了PPR型剪接因子(PBF6、PBF2、ECD2)独立形成剪接复合体的机制,为未来工程化改造叶绿体RNA加工或设计可编程RNA剪接工具提供了潜在靶点。
关键结果: PBF6缺失导致光系统I复合体积累受阻,其与ycf3、clpP1、petB、ndhA、ndhB的内含子结合并剪接;PBF6形成两个独立的多亚基剪接复合体(600 kDa和300 kDa),且三种PPR型剪接因子(PBF6、PBF2、ECD2)通过各自复合体独立促进同一内含子的剪接。
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Nucleus-encoded proteins are involved in intron splicing in plant chloroplasts. Although many splicing factors were discovered, the mechanisms for chloroplast intron splicing remain unknown. Here, we identified a P-class pentatricopeptide repeat (PPR) protein, PHOTOSYSTEM ONE BIOGENESIS FACTOR6 (PBF6), that is essential for the accumulation of photosystem I complex. PBF6 bound to ycf3 intron 1 and clpP1 intron 2, and the introns of petB, ndhA, and ndhB transcripts, and was required for their splicing. Truncated PBF6 containing the 10 N-terminal PPR motifs bound to specific sequences to ycf3 intron 1, clpP1 intron 2, and to the introns of petB, ndhA, and ndhB. PBF6 formed two multi-subunit splicing complexes with other known splicing factors from the CRM, peptidyl-tRNA hydrolase, RNase III, PORR, APO, DEAD-box RNA helicase, and mTERF families. PBF6-containing complex I was about 600 kDa, comprising nine known splicing factors: CAF1, CAF2, CRS2, CFM3a, RNC1, WTF1, APO2, RH3, and mTERF2. PBF6-containing complex II was about 300 kDa and contained three known splicing factors: CAF1, CAF2, and CFM2. Furthermore, two known PPR-type splicing factors, PBF2 and ECD2, both of which are required for splicing the ycf3 intron 1, also formed two multi-subunit splicing complexes with other known splicing factors. Importantly, these three PPR-type splicing factors formed their splicing complexes independently. Our data suggest that a PPR-type splicing factor forms splicing complexes with other known splicing factors under transient expression conditions to facilitate intron splicing and that several PPR-type splicing factors work together to promote the splicing of the same intron through forming respective splicing complexes.