当前细菌基因编码胶囊生物合成蛋白CapI包含由外显子化衍生的核苷酸

Yong Wang, Xia-Fang Tao, Zhixi Su, Ake Liu, Tian-Lei Liu, Ling Sun, Q. Yao, Ke-ping Chen, X. Gu
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引用次数: 4

摘要

自内含子早期假说提出以来,尽管许多研究表明大多数真核生物祖先具有富含内含子的基因组,但细菌祖先基因组中存在内含子的证据仍然缺乏。虽然在当前细菌的所有蛋白质编码基因中没有发现单个内含子,但对古代水平转移到真核生物中的细菌基因的分析可能为细菌祖先存在内含子提供证据。本研究在海葵Nematostella vectensis基因组中发现了一个编码胶囊生物合成蛋白CapI的细菌基因。这个水平转移的基因包含一个40个碱基对的1期内含子。该内含子的核苷酸与当前细菌CapI基因中编码氨基酸的核苷酸具有较高的序列同源性,表明内含子与编码氨基酸的核苷酸同源于同一祖先序列。此外,该内含子的5'剪接位点位于一个GT-poor区域,与紧跟其后的AG-rich区域相关,这表明该内含子被利用5'剪接位点的缺失突变去除,目前细菌CapI基因中的内含子样氨基酸编码核苷酸来源于外显子。这些数据表明,细菌的CapI基因在远古时期就含有内含子。这是第一个提供序列分析结果的报告,表明在祖先细菌基因中可能存在剪接体内含子。本研究中所采用的方法可以用来确定更多这样的证据,这些证据将有助于解决内含子早理论和内含子晚理论之间的争议。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Current Bacterial Gene Encoding Capsule Biosynthesis Protein CapI Contains Nucleotides Derived from Exonization
Since the proposition of introns-early hypothesis, although many studies have shown that most eukaryotic ancestors possessed intron-rich genomes, evidence of intron existence in genomes of ancestral bacteria has still been absent. While not a single intron has been found in all protein-coding genes of current bacteria, analyses on bacterial genes horizontally transferred into eukaryotes at ancient time may provide evidence of intron existence in bacterial ancestors. In this study, a bacterial gene encoding capsule biosynthesis protein CapI was found in the genome of sea anemone, Nematostella vectensis. This horizontally transferred gene contains a phase 1 intron of 40 base pairs. The nucleotides of this intron have high sequence identity with those encoding amino acids in current bacterial CapI gene, indicating that the intron and the amino acid-coding nucleotides are originated from the same ancestor sequence. Moreover, 5'-splice site of this intron is located in a GT-poor region associated with a closely following AG-rich region, suggesting that deletion mutation at 5'-splice site has been employed to remove this intron and the intron-like amino acid-coding nucleotides in current bacterial CapI gene are derived from exonization. These data suggest that bacterial CapI gene contained intron(s) at ancient time. This is the first report providing the result of sequence analysis to suggest possible existence of spliceosomal introns in ancestral bacterial genes. The methodology employed in this study may be used to identify more such evidence that would aid in settlement of the dispute between introns-early and introns-late theories.
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