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2
Relationship between 3' end formation and SL2-specific trans-splicing in polycistronic Caenorhabditis elegans pre-mRNA processing.多顺反子秀丽隐杆线虫前体mRNA加工过程中3'末端形成与SL2特异性反式剪接之间的关系
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Multiple requirements for nematode spliced leader RNP function in trans-splicing.线虫剪接前导RNP在反式剪接中的多种功能需求。
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Comparison of a vitellogenin gene between two distantly related rhabditid nematode species.两种远缘小杆线虫物种间卵黄原蛋白基因的比较。
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Conversion of a trans-spliced C. elegans gene into a conventional gene by introduction of a splice donor site.通过引入剪接供体位点将剪接的秀丽隐杆线虫基因转化为常规基因。
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6
The gut esterase gene (ges-1) from the nematodes Caenorhabditis elegans and Caenorhabditis briggsae.来自秀丽隐杆线虫和布氏隐杆线虫的肠道酯酶基因(ges-1)。
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Trans-splicing of nematode premessenger RNA.线虫前体信使RNA的反式剪接
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Origin, properties, and regulated expression of multiple mRNAs encoded by the protein kinase C1 gene of Caenorhabditis elegans.秀丽隐杆线虫蛋白激酶C1基因编码的多种mRNA的起源、特性及调控表达
J Biol Chem. 1994 May 20;269(20):14820-7.
9
Operons in C. elegans: polycistronic mRNA precursors are processed by trans-splicing of SL2 to downstream coding regions.秀丽隐杆线虫中的操纵子:多顺反子mRNA前体通过SL2与下游编码区的反式剪接进行加工。
Cell. 1993 May 7;73(3):521-32. doi: 10.1016/0092-8674(93)90139-h.
10
The lin-15 locus encodes two negative regulators of Caenorhabditis elegans vulval development.lin-15基因座编码两种秀丽隐杆线虫外阴发育的负调控因子。
Mol Biol Cell. 1994 Apr;5(4):395-411. doi: 10.1091/mbc.5.4.395.

操纵子和SL2反式剪接存在于秀丽隐杆线虫属以外的线虫中。

Operons and SL2 trans-splicing exist in nematodes outside the genus Caenorhabditis.

作者信息

Evans D, Zorio D, MacMorris M, Winter C E, Lea K, Blumenthal T

机构信息

Department of Biology, Indiana University, Bloomington, IN 47405, USA.

出版信息

Proc Natl Acad Sci U S A. 1997 Sep 2;94(18):9751-6. doi: 10.1073/pnas.94.18.9751.

DOI:10.1073/pnas.94.18.9751
PMID:9275196
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC23262/
Abstract

The genomes of most eukaryotes are composed of genes arranged on the chromosomes without regard to function, with each gene transcribed from a promoter at its 5' end. However, the genome of the free-living nematode Caenorhabditis elegans contains numerous polycistronic clusters similar to bacterial operons in which the genes are transcribed sequentially from a single promoter at the 5' end of the cluster. The resulting polycistronic pre-mRNAs are processed into monocistronic mRNAs by conventional 3' end formation, cleavage, and polyadenylation, accompanied by trans-splicing with a specialized spliced leader (SL), SL2. To determine whether this mode of gene organization and expression, apparently unique among the animals, occurs in other species, we have investigated genes in a distantly related free-living rhabditid nematode in the genus Dolichorhabditis (strain CEW1). We have identified both SL1 and SL2 RNAs in this species. In addition, we have sequenced a Dolichorhabditis genomic region containing a gene cluster with all of the characteristics of the C. elegans operons. We show that the downstream gene is trans-spliced to SL2. We also present evidence that suggests that these two genes are also clustered in the C. elegans and Caenorhabditis briggsae genomes. Thus, it appears that the arrangement of genes in operons pre-dates the divergence of the genus Caenorhabditis from the other genera in the family Rhabditidae, and may be more widespread than is currently appreciated.

摘要

大多数真核生物的基因组由排列在染色体上的基因组成,这些基因的排列与功能无关,每个基因都从其5'端的启动子转录而来。然而,自由生活的线虫秀丽隐杆线虫的基因组包含许多类似于细菌操纵子的多顺反子簇,其中基因从簇5'端的单个启动子依次转录。由此产生的多顺反子前体mRNA通过常规的3'端形成、切割和多聚腺苷酸化加工成单顺反子mRNA,并伴随着与特殊剪接前导序列(SL)SL2的反式剪接。为了确定这种在动物中明显独特的基因组织和表达模式是否存在于其他物种中,我们研究了远缘相关的自由生活的杆线虫属(菌株CEW1)中的基因。我们在该物种中鉴定出了SL1和SL2 RNA。此外,我们对一个包含具有秀丽隐杆线虫操纵子所有特征的基因簇的多里杆线虫基因组区域进行了测序。我们表明下游基因与SL2进行反式剪接。我们还提供了证据表明这两个基因在秀丽隐杆线虫和briggsae线虫基因组中也成簇存在。因此,操纵子中的基因排列似乎早于秀丽隐杆线虫属与杆线虫科其他属的分化,并且可能比目前所认识到的更为普遍。