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Gain–of–Function Genetic Models to Study FSH Action

Follicle–stimulating hormone (FSH) is a pituitary-derived gonadotropin that plays key roles in male and female reproduction. The physiology and biochemistry of FSH have been extensively studied for many years. Beginning in the early 1990s, coincident with advances in the then emerging transgenic ani...

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Autores principales: McDonald, Rosemary, Sadler, Carolyn, Kumar, T. Rajendra
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6374295/
https://www.ncbi.nlm.nih.gov/pubmed/30792692
http://dx.doi.org/10.3389/fendo.2019.00028
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author McDonald, Rosemary
Sadler, Carolyn
Kumar, T. Rajendra
author_facet McDonald, Rosemary
Sadler, Carolyn
Kumar, T. Rajendra
author_sort McDonald, Rosemary
collection PubMed
description Follicle–stimulating hormone (FSH) is a pituitary-derived gonadotropin that plays key roles in male and female reproduction. The physiology and biochemistry of FSH have been extensively studied for many years. Beginning in the early 1990s, coincident with advances in the then emerging transgenic animal technology, and continuing till today, several gain-of-function (GOF) models have been developed to understand FSH homeostasis in a physiological context. Our group and others have generated a number of FSH ligand and receptor GOF mouse models. An FSH GOF model when combined with Fshb null mice provides a powerful genetic rescue platform. In this chapter, we discuss different GOF models for FSH synthesis, secretion and action and describe additional novel genetic models that could be developed in the future to further refine the existing models.
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spelling pubmed-63742952019-02-21 Gain–of–Function Genetic Models to Study FSH Action McDonald, Rosemary Sadler, Carolyn Kumar, T. Rajendra Front Endocrinol (Lausanne) Endocrinology Follicle–stimulating hormone (FSH) is a pituitary-derived gonadotropin that plays key roles in male and female reproduction. The physiology and biochemistry of FSH have been extensively studied for many years. Beginning in the early 1990s, coincident with advances in the then emerging transgenic animal technology, and continuing till today, several gain-of-function (GOF) models have been developed to understand FSH homeostasis in a physiological context. Our group and others have generated a number of FSH ligand and receptor GOF mouse models. An FSH GOF model when combined with Fshb null mice provides a powerful genetic rescue platform. In this chapter, we discuss different GOF models for FSH synthesis, secretion and action and describe additional novel genetic models that could be developed in the future to further refine the existing models. Frontiers Media S.A. 2019-02-07 /pmc/articles/PMC6374295/ /pubmed/30792692 http://dx.doi.org/10.3389/fendo.2019.00028 Text en Copyright © 2019 McDonald, Sadler and Kumar. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Endocrinology
McDonald, Rosemary
Sadler, Carolyn
Kumar, T. Rajendra
Gain–of–Function Genetic Models to Study FSH Action
title Gain–of–Function Genetic Models to Study FSH Action
title_full Gain–of–Function Genetic Models to Study FSH Action
title_fullStr Gain–of–Function Genetic Models to Study FSH Action
title_full_unstemmed Gain–of–Function Genetic Models to Study FSH Action
title_short Gain–of–Function Genetic Models to Study FSH Action
title_sort gain–of–function genetic models to study fsh action
topic Endocrinology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6374295/
https://www.ncbi.nlm.nih.gov/pubmed/30792692
http://dx.doi.org/10.3389/fendo.2019.00028
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