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Hex1: a New Human Rad2 Nuclease Family Member with Homology to Yeast Exonuclease 1

Overview
Specialty Biochemistry
Date 1998 Aug 1
PMID 9685493
Citations 47
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Abstract

Nucleolytic processing of chromosomal DNA is required in operations such as DNA repair, recombination and replication. We have identified a human gene, named HEX1 forhumanexonuclease 1, by searching the EST database for cDNAs that encode a homolog to the Saccharomyces cerevisiae EXO1 gene product. Based on its homology to this and other DNA repair proteins of the Rad2 family, most notably Schizosaccharomyces pombe exonuclease 1 (Exo1), Hex1 presumably functions as a nuclease in aspects of recombination or mismatch repair. Similar to the yeast proteins, recombinant Hex1 exhibits a 5'-->3' exonuclease activity. Northern blot analysis revealed that HEX1 expression is highest in fetal liver and adult bone marrow, suggesting that the encoded protein may operate prominently in processes specific to hemopoietic stem cell development. HEX1 gene equivalents were found in all vertebrates examined. The human gene includes 14 exons and 13 introns that span approximately 42 kb of genomic DNA and maps to the chromosomal position 1q42-43, a region lost in some cases of acute leukemia and in several solid tumors.

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References
1.
Breathnach R, Chambon P . Organization and expression of eucaryotic split genes coding for proteins. Annu Rev Biochem. 1981; 50:349-83. DOI: 10.1146/annurev.bi.50.070181.002025. View

2.
Heim S, Teixeira M, Dietrich C, Pandis N . Cytogenetic polyclonality in tumors of the breast. Cancer Genet Cytogenet. 1997; 95(1):16-9. DOI: 10.1016/s0165-4608(96)00322-6. View

3.
Cao L, Alani E, Kleckner N . A pathway for generation and processing of double-strand breaks during meiotic recombination in S. cerevisiae. Cell. 1990; 61(6):1089-101. DOI: 10.1016/0092-8674(90)90072-m. View

4.
Altschul S, Gish W, Miller W, Myers E, Lipman D . Basic local alignment search tool. J Mol Biol. 1990; 215(3):403-10. DOI: 10.1016/S0022-2836(05)80360-2. View

5.
Sun H, Treco D, Szostak J . Extensive 3'-overhanging, single-stranded DNA associated with the meiosis-specific double-strand breaks at the ARG4 recombination initiation site. Cell. 1991; 64(6):1155-61. DOI: 10.1016/0092-8674(91)90270-9. View