A gene-driven approach to the identification of ENU mutants in the mouse

被引:128
作者
Coghill, EL
Hugill, A
Parkinson, N
Davison, C
Glenister, P
Clements, S
Hunter, J
Cox, RD
Brown, SDM [1 ]
机构
[1] MRC, Mammalian Genet Unit, Harwell OX11 0RD, Berks, England
[2] UK Mouse Genome Ctr, Harwell OX11 0RD, Berks, England
[3] GlaxoSmithKline, Harlow CM19 5AW, Essex, England
关键词
D O I
10.1038/ng847
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
The construction of parallel archives of DNA and sperm from mice mutagenized with ethylnitrosurea (ENU) represents a potentially powerful and rapid approach for identifying point mutations in any gene in the mouse genome. We provide support for this approach and report the identification of mutations in the gene (Gjb2) encoding connexin 26, using archives established from the UK ENU mutagenesis program.
引用
收藏
页码:255 / 256
页数:2
相关论文
共 16 条
[1]   Sequence-based analysis of mutagenized mice [J].
Beier, DR .
MAMMALIAN GENOME, 2000, 11 (07) :594-597
[2]   Genotype-based screen for ENU-induced mutations in mouse embryonic stem cells [J].
Chen, YJ ;
Yee, D ;
Dains, K ;
Chatterjee, A ;
Cavalcoli, J ;
Schneider, E ;
Om, J ;
Woychik, RP ;
Magnuson, T .
NATURE GENETICS, 2000, 24 (03) :314-317
[3]   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
[4]   Prelingual deafness: high prevalence of a 30delG mutation in the connexin 26 gene [J].
Denoyelle, F ;
Weil, D ;
Maw, MA ;
Wilcox, SA ;
Lench, NJ ;
AllenPowell, DR ;
Osborn, AH ;
Dahl, HHM ;
Middleton, A ;
Houseman, MJ ;
Dode, C ;
Marlin, S ;
BoulilaElGgaied, A ;
Grati, M ;
Ayadi, H ;
BenArab, S ;
Bitoun, P ;
LinaGranade, G ;
Godet, J ;
Mustapha, M ;
Loiselet, J ;
ElZir, E ;
Aubois, A ;
Joannard, A ;
Levilliers, J ;
Garabedian, EN ;
Mueller, RF ;
Gardner, RJM ;
Petit, C .
HUMAN MOLECULAR GENETICS, 1997, 6 (12) :2173-2177
[5]   Connexin 26 gene linked to a dominant deafness [J].
Denoyelle, F ;
Lina-Granade, G ;
Plauchu, H ;
Bruzzone, R ;
Chaïb, H ;
Lévi-Acobas, F ;
Weil, D ;
Petit, C .
NATURE, 1998, 393 (6683) :319-320
[6]   Comparison of fluorescent single-strand conformation polymorphism analysis and denaturing high-performance liquid chromatography for detection of EXT1 and EXT2 mutations in hereditary multiple exostoses [J].
Dobson-Stone, C ;
Cox, RD ;
Lonie, L ;
Southam, L ;
Fraser, M ;
Wise, C ;
Bernier, F ;
Hodgson, S ;
Porter, DE ;
Simpson, AHRW ;
Monaco, AP .
EUROPEAN JOURNAL OF HUMAN GENETICS, 2000, 8 (01) :24-32
[7]   Connexin-26 mutations in sporadic and inherited sensorineural deafness [J].
Estivill, X ;
Fortina, P ;
Surrey, S ;
Rabionet, R ;
Melchionda, S ;
D'Agruma, L ;
Mansfield, E ;
Rappaport, E ;
Govea, N ;
Milà, M ;
Zelante, L ;
Gasparini, P .
LANCET, 1998, 351 (9100) :394-398
[8]   Transplacental uptake of glucose is decreased in embryonic lethal connexin26-deficient mice [J].
Gabriel, HD ;
Jung, D ;
Bützler, C ;
Temme, A ;
Traub, O ;
Winterhager, E ;
Willecke, K .
JOURNAL OF CELL BIOLOGY, 1998, 140 (06) :1453-1461
[9]   Connexin 26 mutations in hereditary non-syndromic sensorineural deafness [J].
Kelsell, DP ;
Dunlop, J ;
Stevens, HP ;
Lench, NJ ;
Liang, JN ;
Parry, G ;
Mueller, RF ;
Leigh, IM .
NATURE, 1997, 387 (6628) :80-83
[10]   Mouse mutants from chemically mutagenized embryonic stem cells [J].
Munroe, RJ ;
Bergstrom, RA ;
Zheng, QY ;
Libby, B ;
Smith, R ;
John, SWM ;
Schimenti, KJ ;
Browning, VL ;
Schimenti, JC .
NATURE GENETICS, 2000, 24 (03) :318-321