Epithelial-specific Cre/lox recombination in the developing kidney and genitourinary tract

被引:267
作者
Shao, XL
Somlo, S
Igarashi, P
机构
[1] Univ Texas, SW Med Ctr, Dept Internal Med, Div Nephrol, Dallas, TX 75390 USA
[2] Yale Univ, Sch Med, Dept Internal Med, New Haven, CT 06510 USA
[3] Yale Univ, Sch Med, Dept Genet, New Haven, CT 06510 USA
来源
JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY | 2002年 / 13卷 / 07期
关键词
D O I
10.1097/01.ASN.0000016444.90348.50
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Ksp-cadherin is a unique, tissue-specific member of the cadherin family of cell adhesion molecules that is expressed in tubular epithelial cells in the kidney and developing genitourinary (GU) tract. It has recently been shown that a 1341-bp fragment of the 5' flanking region containing the Ksp-cadherin gene promoter can recapitulate the complete expression pattern of the gene in the developing kidney and GU tract. Similar to the endogenous Ksp-cadherin gene, transgenes containing 1341 bp of the 5' flanking region are expressed in developing nephrons, ureteric bud, mesonephric tubules, Wolffian duct, and Mullerian duct. In adult mice, the expression is restricted to renal tubules. In the current study, Ksp1.3/Cre transgenic mice carrying 1329 bp of the Ksp-cadherin 5' flanking region linked to the Cre recombinase gene were produced. Adult transgenic mice expressed Cre recombinase in renal tubules, especially collecting ducts and thick ascending limbs of Henle's loops. Transgenic embryos expressed Cre recombinase in the branching ureteric bud, developing renal tubules, and sex ducts. Ksp1.3/Cre transgenic mice were crossed with mice carrying a lacZ reporter gene that is activated by Cre/lox-mediated genetic recombination. Bitransgenic progeny expressed lacZ exclusively in renal tubules, mesonephric tubules, ureteric bud, developing ureter, and Wolffian duct. These results demonstrate that Ksp1.3/Cre transgenic mice express Cre recombinase exclusively in the kidney and developing GU tract and can mediate epithelial-specific Cre/lox recombination in these tissues. Ksp1.3/Cre transgenic mice should be useful for cell lineage studies and kidney-specific gene targeting.
引用
收藏
页码:1837 / 1846
页数:10
相关论文
共 17 条
  • [1] [Anonymous], 1972, HOUSE MOUSE DEV NORM
  • [2] Eremina V, 2002, J AM SOC NEPHROL, V13, DOI 10.1681/ASN.V133788
  • [3] T-cell-specific deletion of a polypeptide N-acetylgalactosaminyltransferase gene by site-directed recombination
    Hennet, T
    Hagen, FK
    Tabak, LA
    Marth, JD
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (26) : 12070 - 12074
  • [4] HOYER JR, 1974, LAB INVEST, V30, P757
  • [5] Ksp-cadherin gene promoter. II. Kidney-specific activity in transgenic mice
    Igarashi, P
    Shashikant, CS
    Thomson, RB
    Whyte, DA
    Liu-Chen, SX
    Ruddle, FH
    Aronson, PS
    [J]. AMERICAN JOURNAL OF PHYSIOLOGY-RENAL PHYSIOLOGY, 1999, 277 (04) : F599 - F610
  • [6] Jiang XB, 2000, DEVELOPMENT, V127, P1607
  • [7] Nagy A, 2000, GENESIS, V26, P99, DOI 10.1002/(SICI)1526-968X(200002)26:2<99::AID-GENE1>3.0.CO
  • [8] 2-B
  • [9] Expression of an AQP2 Cre recombinase transgene in kidney and male reproductive system of transgenic mice
    Nelson, RD
    Stricklett, P
    Gustafson, C
    Stevens, A
    Ausiello, D
    Brown, D
    Kohan, DE
    [J]. AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY, 1998, 275 (01): : C216 - C226
  • [10] Inducible gene targeting in mice using the Cre/lox system
    Sauer, B
    [J]. METHODS, 1998, 14 (04) : 381 - 392