Keratin 14 Cre transgenic mice authenticate keratin 14 as an oocyte-expressed protein

被引:137
作者
Hafner, M
Wenk, J
Nenci, A
Pasparakis, M
Scharffetter-Kochanek, K
Smyth, N
Peters, T
Kess, D
Holtkötter, O
Shephard, P
Kudlow, JE
Smola, H
Haase, I
Schippers, A
Krieg, T
Müller, W
机构
[1] German Res Ctr Biotechnol, GBF, Dept Expt Immunol, D-38124 Braunschweig, Germany
[2] Univ Cologne, Dept Dermatol, D-5000 Cologne, Germany
[3] Univ Cologne, Dept Dermatol, D-5000 Cologne, Germany
[4] Univ Cologne, Ctr Mol Med, ZMMK, Cologne, Germany
[5] European Mol Biol Lab, Mouse Biol Programme, Monterotondo, Italy
[6] Univ Cologne, Inst Biochem, Cologne, Germany
[7] Nestle Res Ctr, CH-1000 Lausanne, Switzerland
[8] Univ Alabama Birmingham, Div Endocrinol & Metab, Birmingham, AL USA
关键词
Keratin; 14; intermediate filament; Cre recombinase; oocyte; maternal expression;
D O I
10.1002/gene.20016
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Three mouse lines expressing Cre recombinase under the control of the human K14 promoter induced specific deletion of IoxP flanked target sequences in the epidermis, in tongue, and thymic epithelium of the offspring where the Cre allele was inherited from the father. Where the mother carried the Cre allele, IoxP flanked sequences were completely deleted in all tissues of the offspring, even in littermates that did not inherit the Cre allele. This maternally inherited phenotype indicates that the human K14 promoter is transcriptionally active in murine oocytes and that the enzyme remains active until after fertilization, even when the Cre allele becomes transmitted to the polar bodies during meiosis. Detection of K14 mRNA by RT-PCR in murine ovaries and immunohistochemical identification of the K14 protein in oocytes demonstrates that the human K14 promoter behaves like its murine homolog, thus identifying K14 as an authentic oocytic protein. (C) 2004 Wiley-Liss, Inc.
引用
收藏
页码:176 / 181
页数:6
相关论文
共 33 条
[1]   Multipotent cell lineages in early mouse development depend on SOX2 function [J].
Avilion, AA ;
Nicolis, SK ;
Pevny, LH ;
Perez, L ;
Vivian, N ;
Lovell-Badge, R .
GENES & DEVELOPMENT, 2003, 17 (01) :126-140
[2]  
Ayral AM, 1998, TRANSGENICS, V2, P225
[3]   CYTOSKELETAL SHEETS OF MAMMALIAN EGGS AND EMBRYOS - A LATTICE-LIKE NETWORK OF INTERMEDIATE FILAMENTS [J].
CAPCO, DG ;
GALLICANO, GI ;
MCGAUGHEY, RW ;
DOWNING, KH ;
LARABELL, CA .
CELL MOTILITY AND THE CYTOSKELETON, 1993, 24 (02) :85-99
[4]  
de Vries WN, 2000, GENESIS, V26, P110, DOI 10.1002/(SICI)1526-968X(200002)26:2<110::AID-GENE2>3.0.CO
[5]  
2-8
[6]   Genetic control of early folliculogenesis in mice [J].
Epifano, O ;
Dean, J .
TRENDS IN ENDOCRINOLOGY AND METABOLISM, 2002, 13 (04) :169-173
[7]  
FELLENBERG K, 1998, OPTIMIERUNG CREOSTRO
[8]  
GALLICANO GI, 1994, MECH DEVELOP, V45, P211
[9]   DELETION OF A DNA-POLYMERASE-BETA GENE SEGMENT IN T-CELLS USING CELL-TYPE-SPECIFIC GENE TARGETING [J].
GU, H ;
MARTH, JD ;
ORBAN, PC ;
MOSSMANN, H ;
RAJEWSKY, K .
SCIENCE, 1994, 265 (5168) :103-106
[10]   Maternal inheritance of Cre activity in a Sox2Cre deleter train [J].
Hayashi, S ;
Tenzen, T ;
McMahon, AP .
GENESIS, 2003, 37 (02) :51-53