首页> 外文期刊>Journal of Molecular Biology >STRUCTURE AND EXPRESSION OF EUGLENA GRACILIS NUCLEAR RBCS GENES ENCODING THE SMALL SUBUNITS OF THE RIBULOSE 1,5-BISPHOSPHATE CARBOXYLASE OXYGENASE - A NOVEL SPLICING PROCESS FOR UNUSUAL INTERVENING SEQUENCES
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STRUCTURE AND EXPRESSION OF EUGLENA GRACILIS NUCLEAR RBCS GENES ENCODING THE SMALL SUBUNITS OF THE RIBULOSE 1,5-BISPHOSPHATE CARBOXYLASE OXYGENASE - A NOVEL SPLICING PROCESS FOR UNUSUAL INTERVENING SEQUENCES

机译:含核糖1,5-双磷酸羧化酶加氧酶小亚基的Egglena gracilis核RBCS基因的结构和表达-异常插入序列的新剪接过程

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In the protist Euglena gracilis, the small subunit of the chloroplast enzyme ribulose 1,5-bisphosphate carboxylase/oxygenase is encoded by nuclear rbcS genes and synthesized as a polyprotein precursor containing eight mature small subunit molecules. This large precursor is encoded by at least eight different nuclear genes as ascertained by transcript analysis. The structure of three rbcS genes was established and the coding sequences were found to be interrupted by many intervening sequences (IVS). Apart from the first 5' intron involved in trans-splicing, none of these IVSs obeys the GT-AG rule characteristic of introns in higher eukaryote genes. Surprisingly, these IVSs are located at identical positions within the three genes studied. Moreover, extensive sequence homologies were found between IVSs located in the same gene as well as in different genes. The sequences of these homologous IVSs differ only by inserted and/or deleted sequences. The striking conservation of the 5' and 3' regions of these IVSs is correlated to their potential secondary structures. These structures, which bring the IVS extremities together with the exon boundaries, could be involved in a novel splicing process. The second 5' NS is shown to be excised before the addition of the spliced leader sequence to the pre-mRNA. Similarly, two 3' IVSs are excised before the polyadenylation step. These results suggest that IVS splicing is faster than eukaryotic genomic cis-splicing and involves components other than those of the classical spliceosomes. [References: 43]
机译:在原生生物Euglena gracilis中,叶绿体酶核糖1,5-双磷酸羧化酶/加氧酶的小亚基由核rbcS基因编码,并合成为包含八个成熟小亚基分子的多蛋白前体。如转录本分析所确定的,这种大的前体由至少八个不同的核基因编码。建立了三个rbcS基因的结构,发现编码序列被许多插入序列(IVS)中断。除了涉及反式剪接的第一个5'内含子外,这些IVS都没有遵循高级真核生物基因中内含子的GT-AG规则特征。出乎意料的是,这些IVS位于所研究的三个基因内的相同位置。此外,在位于相同基因以及不同基因的IVS之间发现了广泛的序列同源性。这些同源IVS的序列仅在插入和/或缺失的序列上不同。这些IVS的5'和3'区域惊人的保守性与其潜在的二级结构相关。这些将IVS末端与外显子边界结合在一起的结构可能参与了新颖的剪接过程。已显示在将剪接的前导序列添加到pre-mRNA之前已切除了第二个5'NS。类似地,在聚腺苷酸化步骤之前切除两个3'IVS。这些结果表明,IVS剪接比真核基因组顺式剪接更快,并且涉及除经典剪接体以外的其他成分。 [参考:43]

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