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短内含子在鞭毛生物 Euglena gracilis 中获得基质靶向肽中的可能作用。

A possible role for short introns in the acquisition of stroma-targeting peptides in the flagellate Euglena gracilis.

机构信息

Institute of Cell Biology and Biotechnology, Faculty of Natural Sciences, Comenius University, Mlynská dolina, Bratislava, Slovakia.

出版信息

DNA Res. 2010 Aug;17(4):223-31. doi: 10.1093/dnares/dsq015. Epub 2010 Jun 29.

DOI:10.1093/dnares/dsq015
PMID:20587589
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2920757/
Abstract

The chloroplasts of Euglena gracilis bounded by three membranes arose via secondary endosymbiosis of a green alga in a heterotrophic euglenozoan host. Many genes were transferred from symbiont to the host nucleus. A subset of Euglena nuclear genes of predominately symbiont, but also host, or other origin have obtained complex presequences required for chloroplast targeting. This study has revealed the presence of short introns (41-93 bp) either in the second half of presequence-encoding regions or shortly downstream of them in nine nucleus-encoded E. gracilis genes for chloroplast proteins (Eno29, GapA, PetA, PetF, PetJ, PsaF, PsbM, PsbO, and PsbW). In addition, the E. gracilis Pbgd gene contains two introns in the second half of presequence-encoding region and one at the border of presequence-mature peptide-encoding region. Ten of 12 introns present within presequence-encoding regions or shortly downstream of them identified in this study have typical eukaryotic GT/AG borders, are T-rich, 45-50 bp long, and pairwise sequence identities range from 27 to 61%. Thus single recombination events might have been mediated via these cis-spliced introns. A double crossing over between these cis-spliced introns and trans-spliced introns present in 5'-UTRs of Euglena nuclear genes is also likely to have occurred. Thus introns and exon-shuffling could have had an important role in the acquisition of chloroplast targeting signals in E. gracilis. The results are consistent with a late origin of photosynthetic euglenids.

摘要

衣滴虫的叶绿体由三层膜组成,是通过绿藻在异养鞭毛生物宿主中的二次内共生而产生的。许多基因从共生体转移到宿主核内。衣滴虫的一组核基因主要来自共生体,但也有来自宿主或其他来源的基因,它们获得了叶绿体靶向所需的复杂前导序列。这项研究揭示了在九个编码叶绿体蛋白的衣滴虫核基因(ENO29、GAP A、Pet A、Pet F、Pet J、PSA F、PSbM、PSb O 和 PSb W)中,前导序列编码区的后半部分或其后短距离处存在短内含子(41-93bp)。此外,衣滴虫的 Pbgd 基因在前导序列编码区的后半部分和前导序列-成熟肽编码区的边界处含有两个内含子。本研究在编码区的前导序列或其后短距离处鉴定出的 12 个内含子中的 10 个具有典型的真核 GT/AG 边界,富含 T,长度为 45-50bp,序列同一性在 27%到 61%之间。因此,单一重组事件可能是通过这些顺式剪接内含子介导的。这些顺式剪接内含子和 5'-UTR 中转录剪接内含子之间的双交叉也可能发生。因此,内含子和外显子改组可能在衣滴虫获得叶绿体靶向信号中发挥了重要作用。这些结果与光合鞭毛生物的晚期起源相一致。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d4b7/2920757/7fdd7ce9bfae/dsq01501.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d4b7/2920757/7fdd7ce9bfae/dsq01501.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d4b7/2920757/7fdd7ce9bfae/dsq01501.jpg

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