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人类VP16辅助蛋白的基因组组织,一种定位于Xq28的管家基因(HCFC1)。

Genomic organization of the human VP16 accessory protein, a housekeeping gene (HCFC1) mapping to Xq28.

作者信息

Frattini A, Faranda S, Redolfi E, Zucchi I, Villa A, Patrosso M C, Strina D, Susani L, Vezzoni P

机构信息

Istituto di Tecnologie Biomediche Avanzate, Consiglio Nazionale delle Ricerche, Milan, Italy.

出版信息

Genomics. 1994 Sep 1;23(1):30-5. doi: 10.1006/geno.1994.1455.

Abstract

The region between DXS52 and Factor VIII gene in the human Xq28 chromosomal band contains a G+C-rich isochore to which many genes have been mapped. We report here the isolation and characterization of a transcript mapping about 50 kb telomeric from the vasopressin type 2 receptor gene in a 180-kb YACs/cosmid contig containing the L1CAM gene at its centromeric end. The determined transcribed sequence from a human fetal brain library is identical to that of the recently identified accessory protein HCFC1 (host cell factor, also called C1) that activates herpes simplex virus VP16 (alpha TIF) transactivator protein for association with the octamer motif-binding protein Oct-1 (Cell 74: 115, 1993). The gene is expressed in a ubiquitous pattern and a larger transcript of approximately 10 kb is present in all the tissues tested, while an alternatively spliced RNA of approximately 8.0 kb is present in muscle and heart tissues. Genomic sequencing allowed us to determine that the sequenced transcript is assembled from 26 exons spread over a relatively small genomic region of approximately 24 kb. This alllowed us to determine that a previously reported cDNA clone arises from the splicing out of an internal portion of exon 8 which does not change the reading frame. All together these results raise the possibility that alternative mRNA processing could partly contribute to the diversity of the polypeptide HCFC1 family in a subset of tissues.

摘要

人类Xq28染色体带中DXS52与凝血因子VIII基因之间的区域含有一个富含G+C的等臂染色质区,已在其上定位了许多基因。我们在此报告一个转录本的分离与特性分析,该转录本位于一个180 kb的酵母人工染色体/黏粒重叠群中,在距加压素2型受体基因端粒约50 kb处,该重叠群的着丝粒端含有L1CAM基因。从人类胎儿脑文库中确定的转录序列与最近鉴定的辅助蛋白HCFC1(宿主细胞因子,也称为C1)相同,HCFC1可激活单纯疱疹病毒VP16(αTIF)反式激活蛋白,使其与八聚体基序结合蛋白Oct-1结合(《细胞》74:115,1993)。该基因以普遍存在的模式表达,在所检测的所有组织中都存在一个约10 kb的较大转录本,而在肌肉和心脏组织中存在一个约8.0 kb的可变剪接RNA。基因组测序使我们能够确定,测序的转录本由分布在约24 kb相对较小基因组区域的26个外显子组装而成。这使我们能够确定,先前报道的一个cDNA克隆是由外显子8内部部分的剪接产生的,这并未改变阅读框。所有这些结果共同提出了一种可能性,即可变mRNA加工可能在部分组织中对多肽HCFC1家族的多样性有一定贡献。

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