Cloning and Identification of a Novel cDNA Which Encodes a Putative Protein with a DnaJ Domain and a Thioredoxin Active Motif, Human Macrothioredoxin
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- 作者：Shao-Hua Gu ; Jin-Zhong Chen ; Kang Ying ; Shu Wang ; Wei Jin ; Ji Qian ; En-Peng Zhao ; Yi Xie and Yu-Min Mao
- 关键词：human macrothioredoxin (hMTHr) ; thioredoxin ; DnaJ ; chaperone ; splice isoform
- 刊名：Biochemical Genetics
- 出版年：2003
- 出版时间：2003
- 年：2003
- 卷：41
- 期：7/8
- 页码：245-253
- 全文大小：2.98 MB
文摘
A 3345 bp cDNA was isolated from the fetal brain cDNA library by high throughput cDNA sequencing. The cDNA with an open reading fragment (ORF) of 2241 bp encodes a 747 amino acids putative protein with a DnaJ N-terminus domain and four thioredoxin active sets. So it is named human macrothioredoxin (hMTHr). The nucleotide sequences reported in this paper have been deposited in the Genbank database under accession number AF490904 and AY089971. We used Northern blot to detect a band with a length of about 5 kb, which was ubiquitously expressed in human adult tissues with different intensities. The expression pattern was verified by RT-PCR, revealing that the transcripts were ubiquitously expressed in fetal tissues and human tumor tissues also. The transcripts in fetal tissues were more numerous than in adult tissues. The transcripts were high in adult testis, adult pancreas, fetal thymus, and fetal kidney. We have found three splice isoforms with lengths of 3483, 3345, and 2982 bp in the sequencing analysis of the RT-PCR products. They encode three putative proteins with 793, 747, and 275 amino acids, respectively. The first two putative proteins contain a DnaJ domain and four thioredoxin domains. The third putative protein only contains an N-terminus DnaJ domain and one thioredoxin active set. Blast analysis against the NCBI database revealed that the gene spans a genome sequence of about 75 kb that contains at least 25 exons and is located in human chromosome 2q32.1. The organization of the functional motifs of hMTHr suggests that the protein might be a member of a molecular chaperone family.