The expression pattern of PARP-1 and PARP-2 in the developing and adult mouse testis

Acta Histochemica

Volumn 116, Issue 5, 2014, Pages 958-964

  Gungor Ordueri, Nazli Ece ^a   Sahin, Zeliha ^b   Sahin, Pinar ^a   Celik Ozenci, Ciler ^a  

^a AKDENIZ UNIVERSITY   (Turkey)

^b NEAR EAST UNIVERSITY   (Turkey)

Author keywords

Mouse; PARP 1; PARP 2; Testis development

Indexed keywords

NICOTINAMIDE ADENINE DINUCLEOTIDE ADENOSINE DIPHOSPHATE RIBOSYLTRANSFERASE 1; NICOTINAMIDE ADENINE DINUCLEOTIDE ADENOSINE DIPHOSPHATE RIBOSYLTRANSFERASE 2; NICOTINAMIDE ADENINE DINUCLEOTIDE ADENOSINE DIPHOSPHATE RIBOSYLTRANSFERASE; PARP2 PROTEIN, MOUSE;

ADULT; ANIMAL CELL; ANIMAL EXPERIMENT; ANIMAL TISSUE; ARTICLE; BIOTINYLATION; CONTROLLED STUDY; CYTOPLASM; FEMALE; FETUS; IMMUNOHISTOCHEMISTRY; LEYDIG CELL; MALE; MOUSE; NONHUMAN; PROTEIN ANALYSIS; PROTEIN CLEAVAGE; PROTEIN EXPRESSION; PROTEIN FUNCTION; PROTEIN LOCALIZATION; SERTOLI CELL; SPERMATID; SPERMATOGENESIS; SPERMATOGONIUM; TESTIS DEVELOPMENT; ANIMAL; EMBRYOLOGY; GENE EXPRESSION PROFILING; GENE EXPRESSION REGULATION; GENETICS; METABOLISM; TESTIS; WESTERN BLOTTING;

MUS;

ANIMALS; BLOTTING, WESTERN; FEMALE; GENE EXPRESSION PROFILING; GENE EXPRESSION REGULATION, DEVELOPMENTAL; IMMUNOHISTOCHEMISTRY; MALE; MICE; POLY(ADP-RIBOSE) POLYMERASES; TESTIS;

EID: 84904045108     PISSN: 00651281     EISSN: 16180372     Source Type: Journal    
DOI: 10.1016/j.acthis.2014.03.010     Document Type: Article

References (18)

1. Agarwal A., Mahfouz R.Z., Sharma R.K., Sarkar O., Mangrola D., Mathur P.P. Potential biological role of poly(ADP-ribose) polymerase (PARP) in male gametes. Reprod Biol Endocrinol 2009, 7:143.
2. Ame J.C., Rolli V., Schreiber V., Niedergang C., Apiou F., Decker P., et al. PARP-2, a novel mammalian DNA damage-dependent poly(ADP-ribose) polymerase. J Biol Chem 1999, 274:17860-17868.
3. 2 treatment. Eur J Cell Biol 2001, 80:222-229.
4. Dantzer F., Mark M., Quenet D., Scherthan H., Huber A., Liebe B., et al. Poly(ADP-ribose) polymerase-2 contributes to the fidelity of male meiosis I and spermiogenesis. Proc Natl Acad Sci USA 2006, 103:14854-14859.
5. Di Meglio S., Tramontano F., Cimmino G., Jones R., Quesada P. Dual role for poly(ADP-ribose)polymerase-1 and -2 and poly(ADP-ribose)glycohydrolase as DNA-repair and pro-apoptotic factors in rat germinal cells exposed to nitric oxide donors. Biochim Biophys Acta 2004, 1692:35-44.
6. Gobeil S., Boucher C.C., Nadeau D., Poirier G.G. Characterization of the necrotic cleavage of poly(ADP-ribose) polymerase (PARP-1): implication of lysosomal proteases. Cell Death Differ 2001, 8:588-594.
7. Gutti R.K., Tsai-Morris C.H., Dufau M.L. Gonadotropin-regulated testicular helicase (DDX25), an essential regulator of spermatogenesis, prevents testicular germ cell apoptosis. J Biol Chem 2008, 283:17055-17064.
8. Hajkova P., Jeffries S.J., Lee C., Miller N., Jackson S.P., Surani M.A. Genome-wide reprogramming in the mouse germ line entails the base excision repair pathway. Science 2010, 329:78-82.
9. Lau Y.F., Zhang J. Sry interactive proteins: implication for the mechanisms of sex determination. Cytogenet Cell Genet 1998, 80:128-132.
10. Masson M., Niedergang C., Schreiber V., Muller S., Menissier-de Murcia J., de Murcia G. XRCC1 is specifically associated with poly(ADP-ribose) polymerase and negatively regulates its activity following DNA damage. Mol Cell Biol 1998, 18:3563-3571.
11. Messiaen S., Le Bras A., Duquenne C., Barroca V., Moison D., Dechamps N., et al. Rad54 is required for the normal development of male and female germ cells and contributes to the maintainance of their genome integrity after genotoxic stress. Cell Death Dis 2013, 4:e774.
12. Meyer-Ficca M.L., Lonchar J.D., Ihara M., Meistrich M.L., Austin C.A., Meyer R.G. Poly(ADP-ribose) polymerases PARP1 and PARP2 modulate topoisomerase II beta (TOP2B) function during chromatin condensation in mouse spermiogenesis. Biol Reprod 2011, 84:900-909.
13. Rodriguez I., Ody C., Araki K., Garcia I., Vassalli P. An early and massive wave of germinal cell apoptosis is required for the development of functional spermatogenesis. EMBO J 1997, 16:2262-2270.
14. Schreiber V., Ame J.C., Dolle P., Schultz I., Rinaldi B., Fraulob V., et al. Poly(ADP-ribose) polymerase-2 (PARP-2) is required for efficient base excision DNA repair in association with PARP-1 and XRCC1. J Biol Chem 2002, 277:23028-23036.
15. Tramontano F., Malanga M., Quesada P. Differential contribution of poly(ADP-ribose)polymerase-1 and -2 (PARP-1 and -2) to the poly(ADP-ribosyl)ation reaction in rat primary spermatocytes. Mol Hum Reprod 2007, 13:821-828.
16. Wang Z.Q., Stingl L., Morrison C., Jantsch M., Los M., Schulze-Osthoff K., et al. PARP is important for genomic stability but dispensable in apoptosis. Genes Dev 1997, 11:2347-2358.
17. Whitacre C.M., Hashimoto H., Tsai M.L., Chatterjee S., Berger S.J., Berger N.A. Involvement of NAD-poly(ADP-ribose) metabolism in p53 regulation and its consequences. Cancer Res 1995, 55:3697-3701.
18. Xu G.S.G., Mitchell D.L., Mori T., McCarrey J.R., McMahan C.A., et al. Nucleotide excision repair activity varies among murine spermatogenic cell types. Biol Reprod 2005, 73:123-130.