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Isolation of two isoforms of the PAX3 gene transcripts and their tissue-specific alternative expression in human adult tissues.

作者信息

Tsukamoto K, Nakamura Y, Niikawa N

机构信息

Department of Biochemistry, Cancer Institute, Tokyo, Japan.

出版信息

Hum Genet. 1994 Mar;93(3):270-4. doi: 10.1007/BF00212021.

DOI:10.1007/BF00212021
PMID:7545913
Abstract

We have isolated two isoforms of cDNA clones from the human PAX3 gene, a candidate gene responsible for Waardenburg syndrome type I (WSI) as well as a gene associated with development of alveolar rhabdomyosarcoma. The gene product is considered to be one of transcription factors, and the two cDNA clones isolated, termed PAX3A and PAX3B, were generated by alternative splicing. The transcripts coded 215 and 206 amino acids, respectively, and shared 196 amino acids at the NH2 end. The amino acid sequence in the common region (residues 1-196) showed a 100% identity with that of exons 1-4 of the mouse Pax-3 gene. However, both of the PAX3 cDNAs lacked the DNA sequence corresponding to the paired-type homeodomain of the mouse Pax-3 gene. Analysis of gene expression in human adult tissues by reverse transcriptase polymerase chain reaction (RT-PCR) revealed tissue-specific expression of this gene. PAX3B was expressed in most of the tissues examined, but the PAX3A type of transcript was detected only in the cerebellum, esophagus, and skeletal muscle.

摘要

相似文献

1
Isolation of two isoforms of the PAX3 gene transcripts and their tissue-specific alternative expression in human adult tissues.
Hum Genet. 1994 Mar;93(3):270-4. doi: 10.1007/BF00212021.
2
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3
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Am J Hum Genet. 1993 Mar;52(3):455-62.
4
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本文引用的文献

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A new syndrome combining developmental anomalies of the eyelids, eyebrows and nose root with pigmentary defects of the iris and head hair and with congenital deafness.一种新的综合征,其合并了眼睑、眉毛和鼻根的发育异常,虹膜和头部毛发的色素沉着缺陷以及先天性耳聋。
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Mutations in the PAX3 gene causing Waardenburg syndrome type 1 and type 2.PAX3基因的突变导致1型和2型瓦登伯革氏综合征。
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Mutations in the paired domain of the human PAX3 gene cause Klein-Waardenburg syndrome (WS-III) as well as Waardenburg syndrome type I (WS-I).
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Am J Hum Genet. 1993 Mar;52(3):455-62.
4
A mutation within intron 3 of the Pax-3 gene produces aberrantly spliced mRNA transcripts in the splotch (Sp) mouse mutant.Pax-3基因内含子3中的一个突变在斑点(Sp)小鼠突变体中产生异常剪接的mRNA转录本。
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5
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Mutation and cancer: statistical study of retinoblastoma.突变与癌症:视网膜母细胞瘤的统计学研究
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Early retinoic acid-induced F9 teratocarcinoma stem cell gene ERA-1: alternate splicing creates transcripts for a homeobox-containing protein and one lacking the homeobox.早期视黄酸诱导的F9畸胎瘤干细胞基因ERA-1:可变剪接产生含同源异型框蛋白的转录本和一个缺乏同源异型框的转录本。
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