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转钴胺素I(TCN1)染色体基因的基因组结构与定位:与人类内因子的比较

Genomic structure and mapping of the chromosomal gene for transcobalamin I (TCN1): comparison to human intrinsic factor.

作者信息

Johnston J, Yang-Feng T, Berliner N

机构信息

Department of Internal Medicine, Yale University School of Medicine, New Haven, Connecticut 06510.

出版信息

Genomics. 1992 Mar;12(3):459-64. doi: 10.1016/0888-7543(92)90435-u.

Abstract

Transcobalamin I (TCI) is a vitamin B12 binding protein that is found in the secondary granules of mature neutrophils. The expression of the gene for TCI (TCN1) within neutrophils has been shown to be restricted to the later stages of myeloid development and can therefore be used as a marker for granulocyte differentiation. To study transcriptional control regions important in late stage myeloid gene regulation the genomic sequence for TCN1 has been cloned. Clones were isolated from a genomic library constructed in Charon 4A using homologous full-length cDNA probes. Southern blot analysis showed the gene to reside on five EcoRI fragments totaling 14 kb in length. Two overlapping phage clones, containing the entire 14 kb, were isolated and the introns and exons were mapped using Southern blotting and dideoxy sequencing of subclones. The cDNA is represented by nine exons contained within 12 kb of genomic DNA. Comparison of the genomic structure to gastric intrinsic factor (GIF), another vitamin B12 binding protein, revealed a strikingly similar intron/exon structure, with several positionally conserved splice sites. The gene was localized to chromosome 11 using in situ hybridization.

摘要

转钴胺素I(TCI)是一种维生素B12结合蛋白,存在于成熟中性粒细胞的次级颗粒中。已证明中性粒细胞内TCI基因(TCN1)的表达仅限于髓系发育的后期阶段,因此可用作粒细胞分化的标志物。为了研究在髓系基因后期调控中重要的转录控制区域,已克隆了TCN1的基因组序列。使用同源全长cDNA探针从用Charon 4A构建的基因组文库中分离出克隆。Southern印迹分析表明该基因位于五个EcoRI片段上,总长度为14 kb。分离出两个包含整个14 kb的重叠噬菌体克隆,并使用Southern印迹和亚克隆的双脱氧测序对内含子和外显子进行定位。cDNA由基因组DNA 12 kb内的九个外显子代表。将该基因组结构与另一种维生素B12结合蛋白胃内因子(GIF)进行比较,发现其内含子/外显子结构惊人地相似,有几个位置保守的剪接位点。使用原位杂交将该基因定位到11号染色体。

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