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Lin41/Trim71 is essential for mouse development and specifically expressed in postnatal ependymal cells of the brain
Lin41/Trim71 is a heterochronic gene encoding a member of the Trim-NHL protein family, and is the original, genetically defined target of the microRNA let-7 in C. elegans. Both the LIN41 protein and multiple regulatory microRNA binding sites in the 3′ UTR of the mRNA are highly conserved from nemato...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4382986/ https://www.ncbi.nlm.nih.gov/pubmed/25883935 http://dx.doi.org/10.3389/fcell.2015.00020 |
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author | Cuevas, Elisa Rybak-Wolf, Agnieszka Rohde, Anna M. Nguyen, Duong T. T. Wulczyn, F. Gregory |
author_facet | Cuevas, Elisa Rybak-Wolf, Agnieszka Rohde, Anna M. Nguyen, Duong T. T. Wulczyn, F. Gregory |
author_sort | Cuevas, Elisa |
collection | PubMed |
description | Lin41/Trim71 is a heterochronic gene encoding a member of the Trim-NHL protein family, and is the original, genetically defined target of the microRNA let-7 in C. elegans. Both the LIN41 protein and multiple regulatory microRNA binding sites in the 3′ UTR of the mRNA are highly conserved from nematodes to humans. Functional studies have described essential roles for mouse LIN41 in embryonic stem cells, cellular reprogramming and the timing of embryonic neurogenesis. We have used a new gene trap mouse line deficient in Lin41 to characterize Lin41 expression during embryonic development and in the postnatal central nervous system (CNS). In the embryo, Lin41 is required for embryonic viability and neural tube closure. Nevertheless, neurosphere assays suggest that Lin41 is not required for adult neurogenesis. Instead, we show that Lin41 promoter activity and protein expression in the postnatal CNS is restricted to ependymal cells lining the walls of the four ventricles. We use ependymal cell culture to confirm reestablishment of Lin41 expression during differentiation of ependymal progenitors to post-mitotic cells possessing motile cilia. Our results reveal that terminally differentiated ependymal cells express Lin41, a gene to date associated with self-renewing stem cells. |
format | Online Article Text |
id | pubmed-4382986 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-43829862015-04-16 Lin41/Trim71 is essential for mouse development and specifically expressed in postnatal ependymal cells of the brain Cuevas, Elisa Rybak-Wolf, Agnieszka Rohde, Anna M. Nguyen, Duong T. T. Wulczyn, F. Gregory Front Cell Dev Biol Cell and Developmental Biology Lin41/Trim71 is a heterochronic gene encoding a member of the Trim-NHL protein family, and is the original, genetically defined target of the microRNA let-7 in C. elegans. Both the LIN41 protein and multiple regulatory microRNA binding sites in the 3′ UTR of the mRNA are highly conserved from nematodes to humans. Functional studies have described essential roles for mouse LIN41 in embryonic stem cells, cellular reprogramming and the timing of embryonic neurogenesis. We have used a new gene trap mouse line deficient in Lin41 to characterize Lin41 expression during embryonic development and in the postnatal central nervous system (CNS). In the embryo, Lin41 is required for embryonic viability and neural tube closure. Nevertheless, neurosphere assays suggest that Lin41 is not required for adult neurogenesis. Instead, we show that Lin41 promoter activity and protein expression in the postnatal CNS is restricted to ependymal cells lining the walls of the four ventricles. We use ependymal cell culture to confirm reestablishment of Lin41 expression during differentiation of ependymal progenitors to post-mitotic cells possessing motile cilia. Our results reveal that terminally differentiated ependymal cells express Lin41, a gene to date associated with self-renewing stem cells. Frontiers Media S.A. 2015-04-02 /pmc/articles/PMC4382986/ /pubmed/25883935 http://dx.doi.org/10.3389/fcell.2015.00020 Text en Copyright © 2015 Cuevas, Rybak-Wolf, Rohde, Nguyen and Wulczyn. 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) or licensor 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 | Cell and Developmental Biology Cuevas, Elisa Rybak-Wolf, Agnieszka Rohde, Anna M. Nguyen, Duong T. T. Wulczyn, F. Gregory Lin41/Trim71 is essential for mouse development and specifically expressed in postnatal ependymal cells of the brain |
title | Lin41/Trim71 is essential for mouse development and specifically expressed in postnatal ependymal cells of the brain |
title_full | Lin41/Trim71 is essential for mouse development and specifically expressed in postnatal ependymal cells of the brain |
title_fullStr | Lin41/Trim71 is essential for mouse development and specifically expressed in postnatal ependymal cells of the brain |
title_full_unstemmed | Lin41/Trim71 is essential for mouse development and specifically expressed in postnatal ependymal cells of the brain |
title_short | Lin41/Trim71 is essential for mouse development and specifically expressed in postnatal ependymal cells of the brain |
title_sort | lin41/trim71 is essential for mouse development and specifically expressed in postnatal ependymal cells of the brain |
topic | Cell and Developmental Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4382986/ https://www.ncbi.nlm.nih.gov/pubmed/25883935 http://dx.doi.org/10.3389/fcell.2015.00020 |
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