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Expression of a novel brain specific isoform of C3G is regulated during development
Mice lacking C3G (RapGEF1), a ubiquitously expressed protein essential for neuronal differentiation, show multiple defects in brain development. Function of C3G in neurogenesis is poorly defined. Here, we identify brain specific expression of a novel C3G isoform in mice and humans. This isoform has...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7606606/ https://www.ncbi.nlm.nih.gov/pubmed/33139841 http://dx.doi.org/10.1038/s41598-020-75813-z |
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author | Sriram, Divya Chintala, Ramulu Parthasaradhi, B. V. V. Nayak, Sanjeev Chavan Mariappan, Indumathi Radha, Vegesna |
author_facet | Sriram, Divya Chintala, Ramulu Parthasaradhi, B. V. V. Nayak, Sanjeev Chavan Mariappan, Indumathi Radha, Vegesna |
author_sort | Sriram, Divya |
collection | PubMed |
description | Mice lacking C3G (RapGEF1), a ubiquitously expressed protein essential for neuronal differentiation, show multiple defects in brain development. Function of C3G in neurogenesis is poorly defined. Here, we identify brain specific expression of a novel C3G isoform in mice and humans. This isoform has an insert in the Crk-binding region, generating a polypeptide of 175 kDa, unlike the previously known 140 kDa form expressed in all other tissues. In the adult mouse brain, C3G expression is seen in neurons, but was not detectable in GFAP-positive cells. C3G levels were high in the CA3 region of hippocampus and in mitral cells of olfactory bulb. Neural progenitor cells positive for Doublecortin and Nestin, show expression of C3G. During development, C3G is expressed in precursor cells prior to their differentiation into mature neurons or astrocytes. The 175 kDa as well as 140 kDa forms are seen in embryonic mouse brain, while only the 175 kDa variant is seen in post-natal brain. Human cerebral organoids generated from induced pluripotent stem cells predominantly expressed the 140 kDa polypeptides, and the 175 kDa isoform appeared upon maturation. This study describes developmental regulation and neuronal expression of a brain specific isoform of C3G, a molecule essential for normal development of the mammalian brain. |
format | Online Article Text |
id | pubmed-7606606 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-76066062020-11-05 Expression of a novel brain specific isoform of C3G is regulated during development Sriram, Divya Chintala, Ramulu Parthasaradhi, B. V. V. Nayak, Sanjeev Chavan Mariappan, Indumathi Radha, Vegesna Sci Rep Article Mice lacking C3G (RapGEF1), a ubiquitously expressed protein essential for neuronal differentiation, show multiple defects in brain development. Function of C3G in neurogenesis is poorly defined. Here, we identify brain specific expression of a novel C3G isoform in mice and humans. This isoform has an insert in the Crk-binding region, generating a polypeptide of 175 kDa, unlike the previously known 140 kDa form expressed in all other tissues. In the adult mouse brain, C3G expression is seen in neurons, but was not detectable in GFAP-positive cells. C3G levels were high in the CA3 region of hippocampus and in mitral cells of olfactory bulb. Neural progenitor cells positive for Doublecortin and Nestin, show expression of C3G. During development, C3G is expressed in precursor cells prior to their differentiation into mature neurons or astrocytes. The 175 kDa as well as 140 kDa forms are seen in embryonic mouse brain, while only the 175 kDa variant is seen in post-natal brain. Human cerebral organoids generated from induced pluripotent stem cells predominantly expressed the 140 kDa polypeptides, and the 175 kDa isoform appeared upon maturation. This study describes developmental regulation and neuronal expression of a brain specific isoform of C3G, a molecule essential for normal development of the mammalian brain. Nature Publishing Group UK 2020-11-02 /pmc/articles/PMC7606606/ /pubmed/33139841 http://dx.doi.org/10.1038/s41598-020-75813-z Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Sriram, Divya Chintala, Ramulu Parthasaradhi, B. V. V. Nayak, Sanjeev Chavan Mariappan, Indumathi Radha, Vegesna Expression of a novel brain specific isoform of C3G is regulated during development |
title | Expression of a novel brain specific isoform of C3G is regulated during development |
title_full | Expression of a novel brain specific isoform of C3G is regulated during development |
title_fullStr | Expression of a novel brain specific isoform of C3G is regulated during development |
title_full_unstemmed | Expression of a novel brain specific isoform of C3G is regulated during development |
title_short | Expression of a novel brain specific isoform of C3G is regulated during development |
title_sort | expression of a novel brain specific isoform of c3g is regulated during development |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7606606/ https://www.ncbi.nlm.nih.gov/pubmed/33139841 http://dx.doi.org/10.1038/s41598-020-75813-z |
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