Persistent Expression of Notch2 Delays Gonadotrope Differentiation

Author:

Raetzman Lori T.1,Wheeler Bayly S.1,Ross Shelley A.2,Thomas Paul Q.23,Camper Sally A.1

Affiliation:

1. Department of Human Genetics (L.T.R., B.S.W., S.A.C.), University of Michigan, Ann Arbor, Michigan 48109-0638;

2. Murdoch Children’s Research Institute (S.A.R., P.Q.T.), Royal Children’s Hospital, Melbourne, Victoria 3052, Australia;

3. Department of Paediatrics (P.Q.T.), University of Melbourne, Victoria 3010, Australia

Abstract

AbstractNormal pituitary gland development requires coordination between maintenance of progenitor cell pools and selection of progenitors for differentiation. The spatial and temporal expression of Notch2 during pituitary development suggested that it could control progenitor cell differentiation in the pituitary. Consistent with this idea, Notch2 is not expressed in Prop1 mutants, and anterior pituitary progenitors in Prop1 mutants appear to be unable to transition from proliferation to differentiation properly, resulting in anterior lobe failed cell specification and evolving hypoplasia. To test the function of Notch2 directly, we used the αGSU subunit promoter to express activated NOTCH2 persistently in pre-gonadotropes and pre-thyrotropes of transgenic mice. At birth, there is a small reduction in the population of fully differentiated thyrotropes and almost no fully differentiated gonadotropes. The temporal and spatial expression of Hey1 suggests that it could be a mediator of this effect. Gonadotropes complete their differentiation program eventually, although expression of LH and FSH is mutually exclusive with NOTCH2 transgene expression. This demonstrates that activated Notch2 is sufficient to delay gonadotrope differentiation, and it supports the hypothesis that Notch2 regulates progenitor cell differentiation in the pituitary gland.

Publisher

The Endocrine Society

Subject

Endocrinology,Molecular Biology,General Medicine

Reference60 articles.

1. Genetic control of pituitary development and hypopituitarism.;Zhu;Curr Opin Genet Dev,2005

2. How many homeobox genes does it take to make a pituitary gland?;Watkins-Chow;Trends Genet,1998

3. Mutations in PROP1 cause familial combined pituitary hormone deficiency.;Wu;Nat Genet,1998

4. The PROP1 2-base pair deletion is a common cause of combined pituitary hormone deficiency.;Cogan;J Clin Endocrinol Metab,1998

5. Phenotypic variability in familial combined pituitary hormone deficiency Caused by a PROP1 gene mutation resulting in the substitution of Arg-Cys at codon 120 (R120C).;Fluck;J Clin Endocrinol Metab,1998

Cited by 58 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3