PMID- 10644440 OWN - NLM STAT- MEDLINE DCOM- 20000302 LR - 20071114 IS - 0888-7543 (Print) IS - 0888-7543 (Linking) VI - 62 IP - 3 DP - 1999 Dec 15 TI - Characterization of the mouse Xpf DNA repair gene and differential expression during spermatogenesis. PG - 427-35 AB - The human XPF protein, an endonuclease subunit essential for DNA excision repair, may also function in homologous recombination. To investigate a possible link between mammalian XPF and recombination that occurs during meiosis, we isolated, characterized, and determined an expression profile for the mouse Xpf gene. The predicted mouse XPF protein, encoded by a 3.4-kb cDNA, contains 917 amino acids and is 86% identical to human XPF. Appreciable similarity also exists between mouse XPF and homologous proteins in budding yeast (Rad1), fission yeast (Rad16), and fruit fly (Mei-9), all of which have dual functions in excision repair and recombination. Sequence analysis of the 38.3-kb Xpf gene, localized to a region in proximal mouse chromosome 16, revealed greater than 72% identity to human XPF in 16 regions. Of these conserved elements, 11 were exons and 5 were noncoding sequence within introns. Xpf transcript and protein levels were specifically elevated in adult mouse testis. Moreover, increased levels of Xpf and Ercc1 mRNAs correlated with meiotic and early postmeiotic spermatogenic cells. These results support a distinct role for the XPF/ERCC1 junction-specific endonuclease during meiosis, most likely in the resolution of heteroduplex intermediates that arise during recombination. CI - Copyright 1999 Academic Press. FAU - Shannon, M AU - Shannon M AD - Molecular and Structural Biology Division, Lawrence Livermore National Laboratory, Livermore, California 94550, USA. FAU - Lamerdin, J E AU - Lamerdin JE FAU - Richardson, L AU - Richardson L FAU - McCutchen-Maloney, S L AU - McCutchen-Maloney SL FAU - Hwang, M H AU - Hwang MH FAU - Handel, M A AU - Handel MA FAU - Stubbs, L AU - Stubbs L FAU - Thelen, M P AU - Thelen MP LA - eng SI - GENBANK/AF189285 GR - GM52120/GM/NIGMS NIH HHS/United States GR - HD31376/HD/NICHD NIH HHS/United States PT - Journal Article PT - Research Support, U.S. Gov't, Non-P.H.S. PT - Research Support, U.S. Gov't, P.H.S. PL - United States TA - Genomics JT - Genomics JID - 8800135 RN - 0 (DNA, Complementary) RN - 0 (DNA-Binding Proteins) RN - 0 (Proteins) RN - 0 (xeroderma pigmentosum group F protein) RN - EC 3.1.- (Endonucleases) RN - EC 3.1.- (Ercc1 protein, mouse) SB - IM MH - Amino Acid Sequence MH - Animals MH - Chromosome Mapping MH - Cloning, Molecular MH - DNA Repair MH - DNA, Complementary/analysis MH - DNA-Binding Proteins/*biosynthesis/*genetics MH - *Endonucleases MH - *Gene Expression MH - Germ Cells/metabolism MH - Male MH - Mice MH - Molecular Sequence Data MH - Organ Specificity/genetics MH - Proteins/metabolism MH - Sequence Homology, Amino Acid MH - Spermatogenesis/*genetics MH - Testis/metabolism EDAT- 2000/01/25 09:00 MHDA- 2000/03/04 09:00 CRDT- 2000/01/25 09:00 PHST- 2000/01/25 09:00 [pubmed] PHST- 2000/03/04 09:00 [medline] PHST- 2000/01/25 09:00 [entrez] AID - 10.1006/geno.1999.6016 [doi] AID - S0888-7543(99)96016-0 [pii] PST - ppublish SO - Genomics. 1999 Dec 15;62(3):427-35. doi: 10.1006/geno.1999.6016.