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一个位于人类1号染色体末端的新型锌指基因,该基因在人类组织和细胞系中存在可变剪接。

A novel zinc finger gene on human chromosome 1qter that is alternatively spliced in human tissues and cell lines.

作者信息

Saleh M, Selleri L, Evans G A

机构信息

Molecular Genetics Laboratory, Salk Institute for Biological Studies, San Diego, CA 92138.

出版信息

Am J Hum Genet. 1993 Jan;52(1):192-203.

Abstract

DNA-binding proteins that share the conserved C2-H2 zinc finger motif have been shown to have important roles as transcriptional regulators of gene expression and have been implicated in several hereditary human diseases. In order to define potential candidate genes for inherited disorders characterized by aberrant gene expression, we utilized Kruppel-related sequences to isolate zinc finger-containing cDNAs. We isolated and characterized two novel zinc finger-encoding cDNAs from a human hepatoblastoma cell line, which demonstrate DNA sequence homology to a recently described human Kruppel-related gene HZF-3 and appear to be derived from a single gene by alternate mRNA splicing. This gene, denoted "HZF-16," give rise to at least two gene products. One cDNA (i.e., HZF-16.2) has nine zinc finger domains, while alternative splicing of the message gives rise to a smaller product (i.e., HZF-16.1) that has four domains. Despite the internal splicing event, both the 5'- and 3'-untranslated sequences in both cDNAs are identical, as are the first three domains. In the HZF-16.1 cDNA, the fourth zinc finger domain is a fusion product of domains four and nine of HZF-16.2 and could potentially give rise to a new DNA-binding specificity. These alternatively spliced transcripts are differentially regulated in human tissues and transformed cell lines and show a different distribution of expression between human cell lines and normal human tissue. This novel gene was mapped to human chromosome 1q44 by chromosomal in situ suppression hybridization and thus represents a candidate gene for trisomy 1q syndrome and for several other disorders.

摘要

已证明具有保守C2-H2锌指基序的DNA结合蛋白作为基因表达的转录调节因子发挥着重要作用,并与多种人类遗传性疾病有关。为了确定以异常基因表达为特征的遗传性疾病的潜在候选基因,我们利用与克鲁ppel相关的序列来分离含锌指的cDNA。我们从人肝母细胞瘤细胞系中分离并鉴定了两个新的锌指编码cDNA,它们与最近描述的人类克鲁ppel相关基因HZF-3具有DNA序列同源性,并且似乎是通过可变mRNA剪接从单个基因衍生而来。这个基因,命名为“HZF-16”,产生至少两种基因产物。一种cDNA(即HZF-16.2)有九个锌指结构域,而该信使RNA的可变剪接产生一个较小的产物(即HZF-16.1),其有四个结构域。尽管存在内部剪接事件,但两个cDNA中的5'-和3'-非翻译序列是相同的,前三个结构域也是如此。在HZF-16.1 cDNA中,第四个锌指结构域是HZF-16.2的第四和第九个结构域的融合产物,可能会产生一种新的DNA结合特异性。这些可变剪接的转录本在人类组织和转化细胞系中受到不同的调节,并且在人类细胞系和正常人类组织之间表现出不同的表达分布。通过染色体原位抑制杂交将这个新基因定位到人类染色体1q44,因此它代表了1q三体综合征和其他几种疾病的候选基因。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a1b6/1682137/450755c13be8/ajhg00059-0204-a.jpg

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