Genetically engineered mouse models for skin research: Taking the next step

被引:21
作者
Chen, Jiang
Roop, Dennis R. [1 ]
机构
[1] Univ Colorado Denver, Hlth Sci Ctr, Dept Dermatol & Regenerat Med, Aurora, CO 80045 USA
关键词
knock in; knockout; gene targeting; ES cell; targeted mutation; homologus recombination; mouse model; skin;
D O I
10.1016/j.jdermsci.2008.03.012
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
Genetically engineered mouse models are invaluable to investigators in nearly all areas of biomedical research. The use of genetically engineered mice has allowed researchers to explore fundamental functions of genes in a mammal. that shares substantial similarities with human physiology and pathology. Genetically engineered mice are often used as animal models of human diseases that are vital toots in investigating disease development and in developing and testing novel therapies. Gene targeting in embryonic stem cells allows endogenous genes to be specifically altered. As knowledge regarding precise genetic abnormalities underlying a variety of dermatological conditions continues to emerge, the ability to introduce corresponding alterations in endogenous gene loci in mice, often at a single base pair level, has become essential for detailed studies of these genetic diseases. In this review, we provide examples of mouse models harboring modified endogenous gene(s), generated using the technique commonly referred to as the "knock-in" approach, to exemplify the important and sometimes superior rote of this methodology in dermatological research.
引用
收藏
页码:1 / 12
页数:12
相关论文
共 65 条
[1]   TARGETED MUTATION IN THE COL5A2 GENE REVEALS A REGULATORY ROLE FOR TYPE-V COLLAGEN DURING MATRIX ASSEMBLY [J].
ANDRIKOPOULOS, K ;
LIU, X ;
KEENE, DR ;
JAENISCH, R ;
RAMIREZ, F .
NATURE GENETICS, 1995, 9 (01) :31-36
[2]   Focal activation of a mutant allele defines the role of stem cells in mosaic skin disorders [J].
Arin, MJ ;
Longley, MA ;
Wang, XJ ;
Roop, DR .
JOURNAL OF CELL BIOLOGY, 2001, 152 (03) :645-649
[3]   The knockout mouse project [J].
Austin, CP ;
Battey, JF ;
Bradley, A ;
Bucan, M ;
Capecchi, M ;
Collins, FS ;
Dove, WF ;
Duyk, G ;
Dymecki, S ;
Eppig, JT ;
Grieder, FB ;
Heintz, N ;
Hicks, G ;
Insel, TR ;
Joyner, A ;
Koller, BH ;
Lloyd, KCK ;
Magnuson, T ;
Moore, MW ;
Nagy, A ;
Pollock, JD ;
Roses, AD ;
Sands, AT ;
Seed, B ;
Skarnes, WC ;
Snoddy, J ;
Soriano, P ;
Stewart, DJ ;
Stewart, F ;
Stillman, B ;
Varmus, H ;
Varticovski, L ;
Verma, IM ;
Vogt, TF ;
von Melchner, H ;
Witkowski, J ;
Woychik, RP ;
Wurst, W ;
Yancopoulos, GD ;
Young, SG ;
Zambrowicz, B .
NATURE GENETICS, 2004, 36 (09) :921-924
[4]   The European dimension for the mouse genome mutagenesis program [J].
Auwerx, J ;
Avner, P ;
Baldock, R ;
Ballabio, A ;
Balling, R ;
Barbacid, M ;
Berns, A ;
Bradley, A ;
Brown, S ;
Carmeliet, P ;
Chambon, P ;
Cox, R ;
Davidson, D ;
Davies, K ;
Duboule, D ;
Forejt, J ;
Granucci, F ;
Hastie, N ;
de Angelis, MH ;
Jackson, I ;
Kioussis, D ;
Kollias, G ;
Lathrop, M ;
Lendahl, U ;
Malumbres, M ;
von Melchner, H ;
Müller, W ;
Partanen, J ;
Ricciardi-Castagnoli, P ;
Rigby, P ;
Rosen, B ;
Rosenthal, N ;
Skarnes, B ;
Stewart, AF ;
Thornton, J ;
Tocchini-Valentini, G ;
Wagner, E ;
Wahli, W ;
Wurst, W .
NATURE GENETICS, 2004, 36 (09) :925-927
[5]   ACTIVATION OF THE MOUSE CELLULAR HARVEY-RAS GENE IN CHEMICALLY-INDUCED BENIGN SKIN PAPILLOMAS [J].
BALMAIN, A ;
RAMSDEN, M ;
BOWDEN, GT ;
SMITH, J .
NATURE, 1984, 307 (5952) :658-660
[6]  
BARTEK J, 1991, ONCOGENE, V6, P1699
[7]   A transgenic mouse model that recapitulates the clinical features of both neonatal and adult forms of the skin disease epidermolytic hyperkeratosis [J].
Bickenbach, JR ;
Longley, MA ;
Bundman, DS ;
Dominey, AM ;
Bowden, PE ;
Rothnagel, JA ;
Roop, DR .
DIFFERENTIATION, 1996, 61 (02) :129-139
[8]   LINKAGE OF THE EPIDERMOLYTIC HYPERKERATOSIS PHENOTYPE AND THE REGION OF THE TYPE-II KERATIN GENE-CLUSTER ON CHROMOSOME-12 [J].
BONIFAS, JM ;
BARE, JW ;
CHEN, MA ;
LEE, MK ;
SLATER, CA ;
GOLDSMITH, LA ;
EPSTEIN, EH .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 1992, 99 (05) :524-527
[9]  
BOS JL, 1989, CANCER RES, V49, P4682
[10]   An inducible mouse model for epidermolysis bullosa simplex: Implications for gene therapy [J].
Cao, TY ;
Longley, MA ;
Wang, XJ ;
Roop, DR .
JOURNAL OF CELL BIOLOGY, 2001, 152 (03) :651-656