Isolation of cDNA for a novel human protein KNP-I that is homologous to the E. coli SCRP-27A protein from the autoimmune polyglandular disease type I (APECED) region of chromosome 21q22.3

被引:19
作者
Nagamine, K
Kudoh, J
Minoshima, S
Kawasaki, K
Asakawa, S
Ito, F
Shimizu, N
机构
[1] KEIO UNIV,SCH MED,DEPT MOL BIOL,SHINJUKU KU,TOKYO 160,JAPAN
[2] SETSUNAN UNIV,FAC PHARMACEUT SCI,DEPT BIOCHEM,HIRAKATA,OSAKA 57301,JAPAN
基金
日本科学技术振兴机构;
关键词
D O I
10.1006/bbrc.1996.1218
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
We have isolated cDNA clones for a novel human protein KNP-I from fetal brain and bone marrow cDNA libraries. Northern blot analysis indicated that the KNP-I gene is ubiquitously expressed in various human tissues. Significant homology of the KNP-I protein with Escherichia coli anti-sigma cross-reacting protein (SCRP-27A) (44% identity and zebrafish (Brachydanio rerio) es1 protein (49% identity) suggested that thr KNP-I protein may be involved in a basic cellular function, Genomic sequencing revealed that the KNP-I gene consists of seven exons spanning 12 kb. Exon 5 was involved in alternative splicing. The KNP-I gene was mapped between D21S1460 and D21S25 on human chromosome 21q22.3, 26 kb distal to a Not I site of D21S1460. Thus, this novel KNP-I gene could be a candidate gene for autoimmune polyglandular disease type I (APECED) and other disorders mapped to this region. (C) 1996 Academic Press, Inc.
引用
收藏
页码:608 / 616
页数:9
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