Literature DB >> 19332431

Assessment of PARP-3 distribution in tissues of cynomolgous monkeys.

Michèle Rouleau1, Mohamed El-Alfy, Marie-Hélène Lévesque, Guy G Poirier.   

Abstract

Poly(ADP-ribose) polymerase 3 (PARP-3) is a newly characterized PARP. In contrast to the two best-studied nuclear PARPs, PARP-1 and PARP-2, PARP-3 activity is apparently not stimulated by DNA damage. However, our previous work has demonstrated that PARP-3 interacts with several DNA damage response proteins, including Ku70/Ku80, DNA-PK, and PARP-1, suggesting that it contributes to the DNA damage response. Furthermore, a possible function for PARP-3 in the regulation of gene expression has been inferred from our observations that it associates with polycomb group proteins, which are responsible for epigenetic modifications leading to gene silencing. In this report, we extend our characterization of PARP-3 by revealing its distribution in the tissues and cell types of adult cynomolgous monkeys using a well-characterized PARP-3 polyclonal antibody. This study is the first to demonstrate that PARP-3 is genuinely expressed in most of the examined tissues. However, its expression is highly restricted to specific cell types of each tissue, indicating that PARP-3 expression is tightly regulated. One of the key findings of this study is that PARP-3 is highly expressed in the nuclei of epithelial cells forming the ducts of prostate, salivary glands, liver, and pancreas and in the neurons of terminal ganglia.

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Year:  2009        PMID: 19332431      PMCID: PMC2699323          DOI: 10.1369/jhc.2009.953380

Source DB:  PubMed          Journal:  J Histochem Cytochem        ISSN: 0022-1554            Impact factor:   2.479


  16 in total

Review 1.  Poly(ADP-ribosyl)ated chromatin domains: access granted.

Authors:  Michèle Rouleau; Rémy A Aubin; Guy G Poirier
Journal:  J Cell Sci       Date:  2004-02-29       Impact factor: 5.285

Review 2.  Polycomb silencers control cell fate, development and cancer.

Authors:  Anke Sparmann; Maarten van Lohuizen
Journal:  Nat Rev Cancer       Date:  2006-11       Impact factor: 60.716

3.  Intracellular distribution of poly(ADP-ribose) synthetase in rat spermatogenic cells.

Authors:  I I Concha; J Figueroa; M I Concha; K Ueda; L O Burzio
Journal:  Exp Cell Res       Date:  1989-02       Impact factor: 3.905

4.  PARP-3 associates with polycomb group bodies and with components of the DNA damage repair machinery.

Authors:  M Rouleau; D McDonald; P Gagné; M-E Ouellet; A Droit; J M Hunter; S Dutertre; C Prigent; M J Hendzel; G G Poirier
Journal:  J Cell Biochem       Date:  2007-02-01       Impact factor: 4.429

5.  A human poly(ADP-ribose) polymerase gene family (ADPRTL): cDNA cloning of two novel poly(ADP-ribose) polymerase homologues.

Authors:  M Johansson
Journal:  Genomics       Date:  1999-05-01       Impact factor: 5.736

6.  The 630-kb lung cancer homozygous deletion region on human chromosome 3p21.3: identification and evaluation of the resident candidate tumor suppressor genes. The International Lung Cancer Chromosome 3p21.3 Tumor Suppressor Gene Consortium.

Authors:  M I Lerman; J D Minna
Journal:  Cancer Res       Date:  2000-11-01       Impact factor: 12.701

7.  PARP-3 localizes preferentially to the daughter centriole and interferes with the G1/S cell cycle progression.

Authors:  Angélique Augustin; Catherine Spenlehauer; Hélène Dumond; Josiane Ménissier-De Murcia; Matthieu Piel; Anne-Catherine Schmit; Françoise Apiou; Jean-Luc Vonesch; Michael Kock; Michel Bornens; Gilbert De Murcia
Journal:  J Cell Sci       Date:  2003-04-15       Impact factor: 5.285

8.  Cloning and expression of PARP-3 (Adprt3) and U3-55k, two genes closely linked on mouse chromosome 9.

Authors:  P Urbánek; J Paces; J Králová; M Dvorák; V Paces
Journal:  Folia Biol (Praha)       Date:  2002       Impact factor: 0.906

9.  Differential expression of poly(ADP-ribose) polymerase and DNA polymerase beta in rat tissues.

Authors:  M Menegazzi; G Grassi-Zucconi; A Carcerero De Prati; T Ogura; P Poltronieri; H Nyunoya; Y Shiratori-Nyunoya; M Miwa; H Suzuki
Journal:  Exp Cell Res       Date:  1991-11       Impact factor: 3.905

10.  Human Proteinpedia enables sharing of human protein data.

Authors:  Suresh Mathivanan; Mukhtar Ahmed; Natalie G Ahn; Hainard Alexandre; Ramars Amanchy; Philip C Andrews; Joel S Bader; Brian M Balgley; Marcus Bantscheff; Keiryn L Bennett; Erik Björling; Blagoy Blagoev; Ron Bose; Samir K Brahmachari; Alma S Burlingame; Xosé R Bustelo; Gerard Cagney; Greg T Cantin; Helene L Cardasis; Julio E Celis; Raghothama Chaerkady; Feixia Chu; Philip A Cole; Catherine E Costello; Robert J Cotter; David Crockett; James P DeLany; Angelo M De Marzo; Leroi V DeSouza; Eric W Deutsch; Eric Dransfield; Gerard Drewes; Arnaud Droit; Michael J Dunn; Kojo Elenitoba-Johnson; Rob M Ewing; Jennifer Van Eyk; Vitor Faca; Jayson Falkner; Xiangming Fang; Catherine Fenselau; Daniel Figeys; Pierre Gagné; Cecilia Gelfi; Kris Gevaert; Jeffrey M Gimble; Florian Gnad; Renu Goel; Pavel Gromov; Samir M Hanash; William S Hancock; H C Harsha; Gerald Hart; Faith Hays; Fuchu He; Prashantha Hebbar; Kenny Helsens; Heiko Hermeking; Winston Hide; Karin Hjernø; Denis F Hochstrasser; Oliver Hofmann; David M Horn; Ralph H Hruban; Nieves Ibarrola; Peter James; Ole N Jensen; Pia Hønnerup Jensen; Peter Jung; Kumaran Kandasamy; Indu Kheterpal; Reiko F Kikuno; Ulrike Korf; Roman Körner; Bernhard Kuster; Min-Seok Kwon; Hyoung-Joo Lee; Young-Jin Lee; Michael Lefevre; Minna Lehvaslaiho; Pierre Lescuyer; Fredrik Levander; Megan S Lim; Christian Löbke; Joseph A Loo; Matthias Mann; Lennart Martens; Juan Martinez-Heredia; Mark McComb; James McRedmond; Alexander Mehrle; Rajasree Menon; Christine A Miller; Harald Mischak; S Sujatha Mohan; Riaz Mohmood; Henrik Molina; Michael F Moran; James D Morgan; Robert Moritz; Martine Morzel; David C Muddiman; Anuradha Nalli; J Daniel Navarro; Thomas A Neubert; Osamu Ohara; Rafael Oliva; Gilbert S Omenn; Masaaki Oyama; Young-Ki Paik; Kyla Pennington; Rainer Pepperkok; Balamurugan Periaswamy; Emanuel F Petricoin; Guy G Poirier; T S Keshava Prasad; Samuel O Purvine; B Abdul Rahiman; Prasanna Ramachandran; Y L Ramachandra; Robert H Rice; Jens Rick; Ragna H Ronnholm; Johanna Salonen; Jean-Charles Sanchez; Thierry Sayd; Beerelli Seshi; Kripa Shankari; Shi Jun Sheng; Vivekananda Shetty; K Shivakumar; Richard J Simpson; Ravi Sirdeshmukh; K W Michael Siu; Jeffrey C Smith; Richard D Smith; David J States; Sumio Sugano; Matthew Sullivan; Giulio Superti-Furga; Maarit Takatalo; Visith Thongboonkerd; Jonathan C Trinidad; Mathias Uhlen; Joël Vandekerckhove; Julian Vasilescu; Timothy D Veenstra; José-Manuel Vidal-Taboada; Mauno Vihinen; Robin Wait; Xiaoyue Wang; Stefan Wiemann; Billy Wu; Tao Xu; John R Yates; Jun Zhong; Ming Zhou; Yunping Zhu; Petra Zurbig; Akhilesh Pandey
Journal:  Nat Biotechnol       Date:  2008-02       Impact factor: 54.908

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  9 in total

1.  Poly(ADP-ribose) polymerase 3 (PARP3), a newcomer in cellular response to DNA damage and mitotic progression.

Authors:  Christian Boehler; Laurent R Gauthier; Oliver Mortusewicz; Denis S Biard; Jean-Michel Saliou; Anne Bresson; Sarah Sanglier-Cianferani; Susan Smith; Valérie Schreiber; François Boussin; Françoise Dantzer
Journal:  Proc Natl Acad Sci U S A       Date:  2011-01-26       Impact factor: 11.205

2.  PARP-3 is a mono-ADP-ribosylase that activates PARP-1 in the absence of DNA.

Authors:  Olga Loseva; Ann-Sofie Jemth; Helen E Bryant; Herwig Schüler; Lari Lehtiö; Tobias Karlberg; Thomas Helleday
Journal:  J Biol Chem       Date:  2010-01-11       Impact factor: 5.157

3.  A key role for poly(ADP-ribose) polymerase 3 in ectodermal specification and neural crest development.

Authors:  Michèle Rouleau; Vishal Saxena; Amélie Rodrigue; Eric R Paquet; Abbie Gagnon; Michael J Hendzel; Jean-Yves Masson; Marc Ekker; Guy G Poirier
Journal:  PLoS One       Date:  2011-01-17       Impact factor: 3.240

4.  PARP inhibition and the radiosensitizing effects of the PARP inhibitor ABT-888 in in vitro hepatocellular carcinoma models.

Authors:  Clément Guillot; Vincent Favaudon; Zdenko Herceg; Charlotte Sagne; Sylvie Sauvaigo; Philippe Merle; Janet Hall; Isabelle Chemin
Journal:  BMC Cancer       Date:  2014-08-20       Impact factor: 4.430

5.  NAD+ loss, a new player in AhR biology: prevention of thymus atrophy and hepatosteatosis by NAD+ repletion.

Authors:  Silvia Diani-Moore; Jenny Shoots; Rubi Singh; Joshua B Zuk; Arleen B Rifkind
Journal:  Sci Rep       Date:  2017-05-23       Impact factor: 4.379

6.  Characterization of DNA ADP-ribosyltransferase activities of PARP2 and PARP3: new insights into DNA ADP-ribosylation.

Authors:  Gabriella Zarkovic; Ekaterina A Belousova; Ibtissam Talhaoui; Christine Saint-Pierre; Mikhail M Kutuzov; Bakhyt T Matkarimov; Denis Biard; Didier Gasparutto; Olga I Lavrik; Alexander A Ishchenko
Journal:  Nucleic Acids Res       Date:  2018-03-16       Impact factor: 16.971

7.  Dna is a New Target of Parp3.

Authors:  E A Belousova; А A Ishchenko; O I Lavrik
Journal:  Sci Rep       Date:  2018-03-08       Impact factor: 4.379

8.  Poly (ADP-ribose) polymerase 3 (PARP3), a potential repressor of telomerase activity.

Authors:  Tamara Fernández-Marcelo; Cristina Frías; Irene Pascua; Carmen de Juan; Jacqueline Head; Ana Gómez; Florentino Hernando; Jose-Ramon Jarabo; Eduardo Díaz-Rubio; Antonio-Jose Torres; Michèle Rouleau; Manuel Benito; Pilar Iniesta
Journal:  J Exp Clin Cancer Res       Date:  2014-02-15

9.  NF-κB transcriptional activation by TNFα requires phospholipase C, extracellular signal-regulated kinase 2 and poly(ADP-ribose) polymerase-1.

Authors:  Billy Vuong; Adam D J Hogan-Cann; Conrad C Alano; Mackenzie Stevenson; Wai Yee Chan; Christopher M Anderson; Raymond A Swanson; Tiina M Kauppinen
Journal:  J Neuroinflammation       Date:  2015-12-04       Impact factor: 8.322

  9 in total

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