4.0 Article

Pitx2 Deletion in Pituitary Gonadotropes is Compatible With Gonadal Development, Puberty, and Fertility

Journal

GENESIS
Volume 46, Issue 10, Pages 507-514

Publisher

WILEY-LISS
DOI: 10.1002/dvg.20398

Keywords

Cre recombinase; homeobox gene; luteinizing hormone beta subunit; transgenic mice; floxed allele; reproduction; conditional knockout

Funding

  1. NICHD NIH HHS [R01 HD034283, R01 HD034283-12] Funding Source: Medline
  2. NIGMS NIH HHS [T32 GM007544] Funding Source: Medline

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This report introduces a gonadotrope-specific cre transgenic mouse capable of ablating floxed genes in mature pituitary gonadotropes. Initial analysis of this transgenic line, Tg(Lhb-cre)1Sac, reveals that expression is limited to the pituitary cells that produce luteinizing hormone beta, beginning appropriately at e17.5. Cre activity is detectable by a reporter gene in nearly every LH beta-producing cell, but the remaining hormone-producing cell types and other organs exhibit little to no activity. We used the Tg(Lhb-cre)1Sac strain to assess the role Pitx2 in gonadotrope function. The gonadotrope-specific Pitx2 knockout mice exhibit normal expression of LH beta, sexual maturation, and fertility, suggesting that Pitx2 is not required for gonadotrope maintenance or for regulated production of gonadotropins. genesis 46:507-514, 2008. (C) 2008 Wiley-Liss, Inc.

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