4.5 Article

Hypothesis: Trans-splicing Generates Evolutionary Novelty in the Photosynthetic Amoeba Paulinella

期刊

JOURNAL OF PHYCOLOGY
卷 58, 期 3, 页码 392-405

出版社

WILEY
DOI: 10.1111/jpy.13247

关键词

natural selection; Paulinella; photosynthetic eukaryotes; protein truncation; Rhizaria; splice leader; trans-splicing

资金

  1. National Aeronautics and Space Administration [80NSSC19K0462]
  2. NIFA-USDA Hatch grant [NJ01180]

向作者/读者索取更多资源

Plastid primary endosymbiosis occurred twice, leading to massive evolutionary changes. This study focuses on the role of nuclear-derived spliced leader trans-splicing (SLTS) in gene regulation, novel gene origination, and endosymbiont integration in Paulinella micropora KR01. The findings show that 20% of KR01 genes produce transcripts with SL addition sites, resulting in potentially novel functions of truncated proteins. SL addition may facilitate the generation and expression of novel gene variants and enhance the activation and fixation of foreign genes in the host genome of photosynthetic lineages.
Plastid primary endosymbiosis has occurred twice, once in the Archaeplastida ancestor and once in the Paulinella (Rhizaria) lineage. Both events precipitated massive evolutionary changes, including the recruitment and activation of genes that are horizontally acquired (HGT) and the redeployment of existing genes and pathways in novel contexts. Here we address the latter aspect in Paulinella micropora KR01 (hereafter, KR01) that has independently evolved spliced leader (SL) trans-splicing (SLTS) of nuclear-derived transcripts. We investigated the role of this process in gene regulation, novel gene origination, and endosymbiont integration. Our analysis shows that 20% of KR01 genes give rise to transcripts with at least one (but in some cases, multiple) sites of SL addition. This process, which often occurs at canonical cis-splicing acceptor sites (internal introns), results in shorter transcripts that may produce 5 '-truncated proteins with novel functions. SL-truncated transcripts fall into four categories that may show: (i) altered protein localization, (ii) altered protein function, structure, or regulation, (iii) loss of valid alternative start codons, preventing translation, or (iv) multiple SL addition sites at the 5 '-terminus. The SL RNA genes required for SLTS are putatively absent in the heterotrophic sister lineage of photosynthetic Paulinella species. Moreover, a high proportion of transcripts derived from genes of endosymbiotic gene transfer (EGT) and HGT origin contain SL sequences. We hypothesize that truncation of transcripts by SL addition may facilitate the generation and expression of novel gene variants and that SLTS may have enhanced the activation and fixation of foreign genes in the host genome of the photosynthetic lineages, playing a key role in primary endosymbiont integration.

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