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首页> 外文期刊>Genomics >Human eukaryotic initiation factor EIF2C1 gene: cDNA sequence, genomic organization, localization to chromosomal bands 1p34-p35, and expression.
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Human eukaryotic initiation factor EIF2C1 gene: cDNA sequence, genomic organization, localization to chromosomal bands 1p34-p35, and expression.

机译:人类真核生物起始因子EIF2C1基因:cDNA序列,基因组组织,定位于染色体条带1p34-p35和表达。

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摘要

We report the cloning and characterization of the human eukaryotic protein translation initiation factor EIF2C1 gene. The human EIF2C1 gene consists of 19 exons and 18 introns that span a region of almost 50 kb. It is located on the short arm of chromosome 1 in the region 1p34-p35. This genomic region is frequently lost in human cancers such as Wilms tumors, neuroblastoma, and carcinomas of the breast, liver, and colon. The human EIF2C1 gene is ubiquitously expressed at low to medium levels. Differential polyadenylation and splicing result in a complex transcriptional pattern. The cDNA sequence is 7478 bp long and contains an extremely large 3' untranslated region of 4799 bp with multiple, short repeated segments composed of mono-, tri-, or quattronucleotides interspersed throughout. The human EIF2C1 gene belongs to a multigene family in human. It is highly conserved during evolution, sharing about 90% identity with rabbit eIF2C and 70% identity with plant AGO1 at the amino acid level. These facts suggest that human EIF2C1 might play an important physiological role. Copyright 1999 Academic Press.
机译:我们报告了人类真核蛋白翻译起始因子EIF2C1基因的克隆和鉴定。人类EIF2C1基因由19个外显子和18个内含子组成,涵盖了近50 kb的区域。它位于1p34-p35区的1号染色体的短臂上。该基因组区域经常在人类癌症中丢失,例如威尔姆斯肿瘤,成神经细胞瘤以及乳腺癌,肝癌和结肠癌。人类EIF2C1基因在中低水平普遍表达。差异聚腺苷酸化和剪接导致复杂的转录模式。 cDNA序列长为7478 bp,包含一个非常大的3'非翻译区,为4799 bp,具有多个短而重复的,由单核苷酸,三核苷酸或四核苷酸组成的重复片段,贯穿整个片段。人类EIF2C1基因属于人类多基因家族。它在进化过程中是高度保守的,在氨基酸水平上与兔eIF2C具有约90%的同一性,与植物AGO1具有约70%的同一性。这些事实表明,人EIF2C1可能起重要的生理作用。版权所有1999 Academic Press。

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