Haploinsufficiency in mouse models of DNA repair deficiency: modifiers of penetrance

被引:16
作者
Cabelof, Diane C. [1 ]
机构
[1] Wayne State Univ, Dept Nutr & Food Sci, Detroit, MI 48201 USA
关键词
Haploinsufficiency; DNA repair; Heterozygosity; Penetrance; BASE-EXCISION-REPAIR; EARLY EMBRYONIC LETHALITY; POLYMERASE-BETA HAPLOINSUFFICIENCY; SHORTENED LIFE-SPAN; MISMATCH REPAIR; TARGETED DISRUPTION; FANCONI-ANEMIA; GENOMIC STABILITY; HETEROZYGOUS MICE; DAMAGE RESPONSE;
D O I
10.1007/s00018-011-0839-7
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Mouse models of DNA repair deficiency are useful tools for determining susceptibility to disease. Cancer predisposition and premature aging are commonly impacted by deficiencies in DNA repair, presumably as a function of reduced genomic fitness. In this review, a comprehensive analysis of all DNA repair mutant mouse models has been completed in order to assess the importance of haploinsufficiency for these genes. This analysis brings to light a clear role for haploinsufficiency in disease predisposition. Unfortunately, much of the data on heterozygous models are buried or underinvestigated. In light of a better understanding that the role of DNA repair haploinsufficiency may play in penetrance of other oncogenic or disease causing factors, it may be in the interest of human health and disease prevention to further investigate the phenotypes in many of these mouse models.
引用
收藏
页码:727 / 740
页数:14
相关论文
共 83 条
[1]   Mutagenesis Is Elevated in Male Germ Cells Obtained from DNA Polymerase-beta Heterozygous Mice [J].
Allen, Diwi ;
Herbert, Damon C. ;
McMahan, C. Alex ;
Rotrekl, Vladimir ;
Sobol, Robert W. ;
Wilson, Samuel H. ;
Walter, Christi A. .
BIOLOGY OF REPRODUCTION, 2008, 79 (05) :824-831
[2]   Involvement of mouse Mlh1 in DNA mismatch repair and meiotic crossing over [J].
Baker, SM ;
Plug, AW ;
Prolla, TA ;
Bronner, CE ;
Harris, AC ;
Yao, X ;
Christie, DM ;
Monell, C ;
Arnheim, N ;
Bradley, A ;
Ashley, T ;
Liskay, RM .
NATURE GENETICS, 1996, 13 (03) :336-342
[3]  
Baker SM, 1998, CANCER RES, V58, P1087
[4]   MALE-MICE DEFECTIVE IN THE DNA MISMATCH REPAIR GENE PMS2 EXHIBIT ABNORMAL CHROMOSOME SYNAPSIS IN MEIOSIS [J].
BAKER, SM ;
BRONNER, CE ;
ZHANG, L ;
PLUG, AW ;
ROBATZEK, M ;
WARREN, G ;
ELLIOTT, EA ;
YU, JA ;
ASHLEY, T ;
ARNHEIM, N ;
FLAVELL, RA ;
LISKAY, RM .
CELL, 1995, 82 (02) :309-319
[5]   Fancm-deficient mice reveal unique features of Fanconi anemia complementation group M [J].
Bakker, Sietske T. ;
van de Vrugt, Henri J. ;
Rooimans, Martin A. ;
Oostra, Anneke B. ;
Steltenpool, Jurgen ;
Delzenne-Goette, Elly ;
van der Wal, Anja ;
van der Valk, Martin ;
Joenje, Hans ;
te Riele, Hein ;
de Winter, Johan P. .
HUMAN MOLECULAR GENETICS, 2009, 18 (18) :3484-3495
[6]   Repair and genetic consequences of endogenous DNA base damage in mammalian cells [J].
Barnes, DE ;
Lindahl, T .
ANNUAL REVIEW OF GENETICS, 2004, 38 :445-476
[7]   DNA damage response as an anti-cancer barrier - Damage threshold and the concept of 'conditional haploinsufficiency' [J].
Bartek, Jiri ;
Lukas, Jiri ;
Bartkova, Jirina .
CELL CYCLE, 2007, 6 (19) :2344-2347
[8]   Beyond ATM: The protein kinase landscape of the DNA damage response [J].
Bensimon, Ariel ;
Aebersold, Ruedi ;
Shiloh, Yosef .
FEBS LETTERS, 2011, 585 (11) :1625-1639
[9]  
Brown EJ, 2000, GENE DEV, V14, P397
[10]   Imbalanced base excision repair in response to folate deficiency is accelerated by polymerase β haploinsufficiency [J].
Cabelof, DC ;
Raffoul, JJ ;
Nakamura, J ;
Kapoor, D ;
Abdalla, H ;
Heydari, AR .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2004, 279 (35) :36504-36513