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Survival of glucose phosphate isomerase null somatic cells and germ cells in adult mouse chimaeras

The mouse Gpi1 gene encodes the glycolytic enzyme glucose phosphate isomerase. Homozygous Gpi1(−/−) null mouse embryos die but a previous study showed that some homozygous Gpi1(−/−) null cells survived when combined with wild-type cells in fetal chimaeras. One adult female Gpi1(−/−)↔Gpi1(c/c) chimae...

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Autores principales: Keighren, Margaret A., Flockhart, Jean H., West, John D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Company of Biologists Ltd 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4874354/
https://www.ncbi.nlm.nih.gov/pubmed/27103217
http://dx.doi.org/10.1242/bio.017111
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author Keighren, Margaret A.
Flockhart, Jean H.
West, John D.
author_facet Keighren, Margaret A.
Flockhart, Jean H.
West, John D.
author_sort Keighren, Margaret A.
collection PubMed
description The mouse Gpi1 gene encodes the glycolytic enzyme glucose phosphate isomerase. Homozygous Gpi1(−/−) null mouse embryos die but a previous study showed that some homozygous Gpi1(−/−) null cells survived when combined with wild-type cells in fetal chimaeras. One adult female Gpi1(−/−)↔Gpi1(c/c) chimaera with functional Gpi1(−/−) null oocytes was also identified in a preliminary study. The aims were to characterise the survival of Gpi1(−/−) null cells in adult Gpi1(−/−)↔Gpi1(c/c) chimaeras and determine if Gpi1(−/−) null germ cells are functional. Analysis of adult Gpi1(−/−)↔Gpi1(c/c) chimaeras with pigment and a reiterated transgenic lineage marker showed that low numbers of homozygous Gpi1(−/−) null cells could survive in many tissues of adult chimaeras, including oocytes. Breeding experiments confirmed that Gpi1(−/−) null oocytes in one female Gpi1(−/−)↔Gpi1(c/c) chimaera were functional and provided preliminary evidence that one male putative Gpi1(−/−)↔Gpi1(c/c) chimaera produced functional spermatozoa from homozygous Gpi1(−/−) null germ cells. Although the male chimaera was almost certainly Gpi1(−/−)↔Gpi1(c/c), this part of the study is considered preliminary because only blood was typed for GPI. Gpi1(−/−) null germ cells should survive in a chimaeric testis if they are supported by wild-type Sertoli cells. It is also feasible that spermatozoa could bypass a block at GPI, but not blocks at some later steps in glycolysis, by using fructose, rather than glucose, as the substrate for glycolysis. Although chimaera analysis proved inefficient for studying the fate of Gpi1(−/−) null germ cells, it successfully identified functional Gpi1(−/−) null oocytes and revealed that some Gpi1(−/−) null cells could survive in many adult tissues.
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spelling pubmed-48743542016-06-02 Survival of glucose phosphate isomerase null somatic cells and germ cells in adult mouse chimaeras Keighren, Margaret A. Flockhart, Jean H. West, John D. Biol Open Research Article The mouse Gpi1 gene encodes the glycolytic enzyme glucose phosphate isomerase. Homozygous Gpi1(−/−) null mouse embryos die but a previous study showed that some homozygous Gpi1(−/−) null cells survived when combined with wild-type cells in fetal chimaeras. One adult female Gpi1(−/−)↔Gpi1(c/c) chimaera with functional Gpi1(−/−) null oocytes was also identified in a preliminary study. The aims were to characterise the survival of Gpi1(−/−) null cells in adult Gpi1(−/−)↔Gpi1(c/c) chimaeras and determine if Gpi1(−/−) null germ cells are functional. Analysis of adult Gpi1(−/−)↔Gpi1(c/c) chimaeras with pigment and a reiterated transgenic lineage marker showed that low numbers of homozygous Gpi1(−/−) null cells could survive in many tissues of adult chimaeras, including oocytes. Breeding experiments confirmed that Gpi1(−/−) null oocytes in one female Gpi1(−/−)↔Gpi1(c/c) chimaera were functional and provided preliminary evidence that one male putative Gpi1(−/−)↔Gpi1(c/c) chimaera produced functional spermatozoa from homozygous Gpi1(−/−) null germ cells. Although the male chimaera was almost certainly Gpi1(−/−)↔Gpi1(c/c), this part of the study is considered preliminary because only blood was typed for GPI. Gpi1(−/−) null germ cells should survive in a chimaeric testis if they are supported by wild-type Sertoli cells. It is also feasible that spermatozoa could bypass a block at GPI, but not blocks at some later steps in glycolysis, by using fructose, rather than glucose, as the substrate for glycolysis. Although chimaera analysis proved inefficient for studying the fate of Gpi1(−/−) null germ cells, it successfully identified functional Gpi1(−/−) null oocytes and revealed that some Gpi1(−/−) null cells could survive in many adult tissues. The Company of Biologists Ltd 2016-04-21 /pmc/articles/PMC4874354/ /pubmed/27103217 http://dx.doi.org/10.1242/bio.017111 Text en © 2016. Published by The Company of Biologists Ltd http://creativecommons.org/licenses/by/3.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0), which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed.
spellingShingle Research Article
Keighren, Margaret A.
Flockhart, Jean H.
West, John D.
Survival of glucose phosphate isomerase null somatic cells and germ cells in adult mouse chimaeras
title Survival of glucose phosphate isomerase null somatic cells and germ cells in adult mouse chimaeras
title_full Survival of glucose phosphate isomerase null somatic cells and germ cells in adult mouse chimaeras
title_fullStr Survival of glucose phosphate isomerase null somatic cells and germ cells in adult mouse chimaeras
title_full_unstemmed Survival of glucose phosphate isomerase null somatic cells and germ cells in adult mouse chimaeras
title_short Survival of glucose phosphate isomerase null somatic cells and germ cells in adult mouse chimaeras
title_sort survival of glucose phosphate isomerase null somatic cells and germ cells in adult mouse chimaeras
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4874354/
https://www.ncbi.nlm.nih.gov/pubmed/27103217
http://dx.doi.org/10.1242/bio.017111
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