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

Citation
H. Kamma et al., Interaction of hnRNP A2/B1 isoforms with telomeric ssDNA and the in vitro function, BIOC BIOP R, 280(3), 2001, pp. 625-630
Citations number
23
Categorie Soggetti
Biochemistry & Biophysics
Journal title
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS
ISSN journal
0006291X → ACNP
Volume
280
Issue
3
Year of publication
2001
Pages
625 - 630
Database
ISI
SICI code
0006-291X(20010126)280:3<625:IOHAIW>2.0.ZU;2-M
Abstract
Overexpression of heterogeneous nuclear ribonucleoprotein (hnRNP) A2/B1, es pecially of B1 has been reported as a useful marker to detect cancers in ea rly 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 min or 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 telome ric single-stranded DNA (ssDNA) than A2 and B0a. Kinetic analyses using pur ified B1 and B0b indicated that they interact dynamically with a single arr ay of telomeric repeats. Furthermore, functional assays demonstrated that B 1 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.