Reproductive Function in Protein Kinase Inhibitor-Deficient Mice

Author:

Belyamani Mouna12,Gangolli Esha A.12,Idzerda Rejean L.132

Affiliation:

1. Department of Medicine, Division of Metabolism, Endocrinology and Nutrition 1 and

2. Veterans Affairs Puget Sound Health Care System, Seattle, Washington 981082

3. Department of Pharmacology, 3 University of Washington, Seattle, Washington 98195, and

Abstract

ABSTRACT The protein kinase inhibitor (PKI) family includes three genes encoding small, heat-stable inhibitors of the cyclic AMP-dependent kinase PKA. Each PKI isoform contains a PKA inhibitory domain and a nuclear export domain, enabling PKI to both inhibit PKA and remove it from the nucleus. The PKIβ isoform, also known as testis PKI, is highly expressed in germ cells of the testis and is found at more modest levels in other tissues. In order to investigate its physiological role, we have generated PKIβ knockout mice by gene targeting. These mice exhibit a partial loss of PKI activity in testis but remain fertile with normal testis development and function. PKIβ knockout females also reproduce normally. The PKIβ mutants were crossed with our previously derived PKIα mutants to obtain double-knockout mice. Remarkably, these mice are also viable and fertile with no obvious physiological defects in either males or females.

Publisher

American Society for Microbiology

Subject

Cell Biology,Molecular Biology

Reference24 articles.

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