New semidominant mutations that affect mouse development

被引:23
作者
Bogani, D
Warr, N
Elms, P
Davies, J
Tymowska-Lalanne, Z
Goldsworthy, M
Cox, RD
Keays, DA
Flint, J
Wilson, V
Nolan, P
Arkell, R [1 ]
机构
[1] MRC Harwell, Mammalian Genet Unit, Lab Early Dev, Didcot OX11 0RD, Oxon, England
[2] Mammalian Genet Unit, Genotyping & Mutat Detect, Didcot, Oxon, England
[3] Mammalian Genet Unit, Diabet Grp, Didcot, Oxon, England
[4] Wellcome Trust Ctr Human Genet, Psychiat Genet Lab, Oxford, England
[5] Inst Stem Cell Res, Edinburgh, Midlothian, Scotland
基金
英国医学研究理事会;
关键词
ENU; mouse gastrulation; Pax3; brachyury; Wnt3a;
D O I
10.1002/gene.20071
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Dominantly acting mutations that produce visible phenotypes are frequently recovered, either during routine maintenance of colonies or from mutagenesis experiments. We have studied 12 dominant mouse mutations that cause a tail dysmorphology, a coat spotting phenotype, or a combination of these. The majority of these mutations act in a semidominant manner with the homozygous state associated with embryonic lethality and a visible phenotype at or before midgestation. The homozygous phenotypes include axis truncation and neural crest cell defects, as may be expected from the heterozygous phenotypes. The majority of mutations, however, also produced other phenotypes that include neural tube closure defects and aberrant heart looping. In one coat spotting mutant the homozygous condition is lethal before neural crest cell production commences. The mutated genes often function in processes additional to those alluded to by the heterozygous phenotype. (C) 2004 Wiley-Liss, Inc.
引用
收藏
页码:109 / 117
页数:9
相关论文
共 23 条
[1]   MGD: the Mouse Genome Database [J].
Blake, JA ;
Richardson, JE ;
Bult, RJ ;
Kadin, JA ;
Eppig, JT .
NUCLEIC ACIDS RESEARCH, 2003, 31 (01) :193-195
[2]   The X-linked mouse mutation Bent tail is associated with a deletion of the Zic3 locus [J].
Carrel, T ;
Purandare, SM ;
Harrison, W ;
Elder, F ;
Fox, T ;
Casey, B ;
Herman, GE .
HUMAN MOLECULAR GENETICS, 2000, 9 (13) :1937-1942
[3]   Crooked tail (Cd) models human folate-responsive neural tube defects [J].
Carter, M ;
Ulrich, S ;
Oofuji, Y ;
Williams, DA ;
Ross, ME .
HUMAN MOLECULAR GENETICS, 1999, 8 (12) :2199-2204
[4]  
CATTANACH BM, 1987, MOUSE NEWS LETT, V77, P122
[5]  
Conlon FL, 1996, DEVELOPMENT, V122, P2427
[6]   Genome-wide, large-scale production of mutant mice by ENU mutagenesis [J].
de Angelis, MH ;
Flaswinkel, H ;
Fuchs, H ;
Rathkolb, B ;
Soewarto, D ;
Marschall, S ;
Heffner, S ;
Pargent, W ;
Wuensch, K ;
Jung, M ;
Reis, A ;
Richter, T ;
Alessandrini, F ;
Jakob, T ;
Fuchs, E ;
Kolb, H ;
Kremmer, E ;
Schaeble, K ;
Rollinski, B ;
Roscher, A ;
Peters, C ;
Meitinger, T ;
Strom, T ;
Steckler, T ;
Holsboer, F ;
Klopstock, T ;
Gekeler, F ;
Schindewolf, C ;
Jung, T ;
Avraham, K ;
Behrendt, H ;
Ring, J ;
Zimmer, A ;
Schughart, K ;
Pfeffer, K ;
Wolf, E ;
Balling, R .
NATURE GENETICS, 2000, 25 (04) :444-447
[7]   Zic2 is required for neural crest formation and hindbrain patterning during mouse development [J].
Elms, P ;
Siggers, P ;
Napper, D ;
Greenfield, A ;
Arkell, R .
DEVELOPMENTAL BIOLOGY, 2003, 264 (02) :391-406
[8]   SPLOTCH (SP2H), A MUTATION AFFECTING DEVELOPMENT OF THE MOUSE NEURAL-TUBE, SHOWS A DELETION WITHIN THE PAIRED HOMEODOMAIN OF PAX-3 [J].
EPSTEIN, DJ ;
VEKEMANS, M ;
GROS, P .
CELL, 1991, 67 (04) :767-774
[9]   Analysis of the vestigial tail mutation demonstrates that Wnt-3a gene dosage regulates mouse axial development [J].
Greco, TL ;
Takada, S ;
Newhouse, MM ;
McMahon, TA ;
McMahon, AP ;
Camper, SA .
GENES & DEVELOPMENT, 1996, 10 (03) :313-324
[10]  
GRUNEBERG H, 1958, J EMBRYOL EXP MORPH, V6, P424