Interaction of hnRNP A2/B1 isoforms with telomeric ssDNA and the in vitro function

被引:57
作者
Kamma, H [1 ]
Fujimoto, M
Fujiwara, M
Matsui, M
Horiguchi, H
Hamasaki, M
Satoh, H
机构
[1] Univ Tsukuba, Inst Basic Med Sci, Ibaraki, Osaka 3058575, Japan
[2] Kensei Gen Hosp, Ibaraki, Osaka 3091295, Japan
[3] Ibaraki Prefectural Univ Hlth Sci, Ctr Med Sci, Ibaraki, Osaka 3000331, Japan
[4] Univ Tsukuba, Inst Clin Med, Ibaraki, Osaka 3058575, Japan
关键词
hnRNP B1; hnRNP BOb; telomere; single-stranded DNA; telomerase;
D O I
10.1006/bbrc.2000.4173
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
Overexpression of heterogeneous nuclear ribonucleoprotein (hnRNP) A2/B1, especially of B1 has been reported as a useful marker to detect cancers in early stage, although the biological reason is not clear. A2/B1 proteins were previously reported to bind telomeric DNA repeats. Alternative splicing of A2/B1 gene produces abundant A2, less abundant B1, and testis-specific minor isoforms B0a and B0b. In this study, B1 and B0b that have the N-terminal 12 amino acid insertion were suggested to have higher affinities to telomeric single-stranded DNA (ssDNA) than A2 and B0a. Kinetic analyses using purified B1 and B0b indicated that they interact dynamically with a single array of telomeric repeats. Furthermore, functional assays demonstrated that B1 and B0b bind with telomeric repeats in a tandem fashion and protect them from a nuclease and promote telomerase activity. A2/B1 proteins, especially B1 and B0b, may function as telomeric ssDNA-binding proteins in cancer and reproductive cells, (C) 2001 Academic Press.
引用
收藏
页码:625 / 630
页数:6
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