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Differential LINE-1 regulation in pluripotent stem cells of humans and other great apes

Identifying cellular and molecular differences between human and non-human primates (NHPs) is essential to the basic understanding of the evolution and diversity of our own species. Until now, preserved tissues have been the main source for most comparative studies between humans, chimpanzees (Pan t...

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Autores principales: Marchetto, Maria C. N., Narvaiza, Iñigo, Denli, Ahmet M., Benner, Christopher, Lazzarini, Thomas A., Nathanson, Jason L., Paquola, Apuã C. M., Desai, Keval N., Herai, Roberto H., Weitzman, Matthew D., Yeo, Gene W., Muotri, Alysson R., Gage, Fred H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4064720/
https://www.ncbi.nlm.nih.gov/pubmed/24153179
http://dx.doi.org/10.1038/nature12686
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author Marchetto, Maria C. N.
Narvaiza, Iñigo
Denli, Ahmet M.
Benner, Christopher
Lazzarini, Thomas A.
Nathanson, Jason L.
Paquola, Apuã C. M.
Desai, Keval N.
Herai, Roberto H.
Weitzman, Matthew D.
Yeo, Gene W.
Muotri, Alysson R.
Gage, Fred H.
author_facet Marchetto, Maria C. N.
Narvaiza, Iñigo
Denli, Ahmet M.
Benner, Christopher
Lazzarini, Thomas A.
Nathanson, Jason L.
Paquola, Apuã C. M.
Desai, Keval N.
Herai, Roberto H.
Weitzman, Matthew D.
Yeo, Gene W.
Muotri, Alysson R.
Gage, Fred H.
author_sort Marchetto, Maria C. N.
collection PubMed
description Identifying cellular and molecular differences between human and non-human primates (NHPs) is essential to the basic understanding of the evolution and diversity of our own species. Until now, preserved tissues have been the main source for most comparative studies between humans, chimpanzees (Pan troglodytes) and bonobos (Pan paniscus)(1,2). However, these tissue samples do not fairly represent the distinctive traits of live cell behavior and are not amenable to genetic manipulation. We hypothesized that induced pluripotent stem cells (iPSCs) could be a unique biological resource to elucidate relevant phenotypical differences between human and NHPs and that those differences could have potential adaptation and speciation value. Here, we describe the generation and initial characterization of iPSCs from chimpanzees and bonobos as novel tools to explore factors that have contributed to great ape evolution. Comparative gene expression analysis of human and NHP iPSCs revealed differences in the regulation of Long Interspersed Nuclear Element-1 (LINE-1 or L1) transposons. A force of change in mammalian evolution, L1 elements are retrotransposons that have remained active during primate evolution(3-5). Decreased levels of L1 restricting factors APOBEC3B (A3B)(6) and PIWIL2(7) in NHP iPSCs correlated with increased L1 mobility and endogenous L1 mRNA levels. Moreover, results from manipulation of A3B and PIWIL2 levels in iPSCs supported a causal inverse relationship between levels of these proteins and L1 retrotransposition. Finally, we found increased copy numbers of species-specific L1 elements in the genome of chimpanzees compared to humans, supporting the idea that increased L1 mobility in NHPs is not limited to iPSCs in culture and may have also occurred in the germline or embryonic cells developmentally upstream to germline specification during primate evolution. We propose that differences in L1 mobility may have differentially shaped the genomes of humans and NHPs and could have ongoing adaptive significance.
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spelling pubmed-40647202014-06-20 Differential LINE-1 regulation in pluripotent stem cells of humans and other great apes Marchetto, Maria C. N. Narvaiza, Iñigo Denli, Ahmet M. Benner, Christopher Lazzarini, Thomas A. Nathanson, Jason L. Paquola, Apuã C. M. Desai, Keval N. Herai, Roberto H. Weitzman, Matthew D. Yeo, Gene W. Muotri, Alysson R. Gage, Fred H. Nature Article Identifying cellular and molecular differences between human and non-human primates (NHPs) is essential to the basic understanding of the evolution and diversity of our own species. Until now, preserved tissues have been the main source for most comparative studies between humans, chimpanzees (Pan troglodytes) and bonobos (Pan paniscus)(1,2). However, these tissue samples do not fairly represent the distinctive traits of live cell behavior and are not amenable to genetic manipulation. We hypothesized that induced pluripotent stem cells (iPSCs) could be a unique biological resource to elucidate relevant phenotypical differences between human and NHPs and that those differences could have potential adaptation and speciation value. Here, we describe the generation and initial characterization of iPSCs from chimpanzees and bonobos as novel tools to explore factors that have contributed to great ape evolution. Comparative gene expression analysis of human and NHP iPSCs revealed differences in the regulation of Long Interspersed Nuclear Element-1 (LINE-1 or L1) transposons. A force of change in mammalian evolution, L1 elements are retrotransposons that have remained active during primate evolution(3-5). Decreased levels of L1 restricting factors APOBEC3B (A3B)(6) and PIWIL2(7) in NHP iPSCs correlated with increased L1 mobility and endogenous L1 mRNA levels. Moreover, results from manipulation of A3B and PIWIL2 levels in iPSCs supported a causal inverse relationship between levels of these proteins and L1 retrotransposition. Finally, we found increased copy numbers of species-specific L1 elements in the genome of chimpanzees compared to humans, supporting the idea that increased L1 mobility in NHPs is not limited to iPSCs in culture and may have also occurred in the germline or embryonic cells developmentally upstream to germline specification during primate evolution. We propose that differences in L1 mobility may have differentially shaped the genomes of humans and NHPs and could have ongoing adaptive significance. 2013-10-23 2013-11-28 /pmc/articles/PMC4064720/ /pubmed/24153179 http://dx.doi.org/10.1038/nature12686 Text en Users may view, print, copy, download and text and data- mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use: http://www.nature.com/authors/editorial_policies/license.html#terms
spellingShingle Article
Marchetto, Maria C. N.
Narvaiza, Iñigo
Denli, Ahmet M.
Benner, Christopher
Lazzarini, Thomas A.
Nathanson, Jason L.
Paquola, Apuã C. M.
Desai, Keval N.
Herai, Roberto H.
Weitzman, Matthew D.
Yeo, Gene W.
Muotri, Alysson R.
Gage, Fred H.
Differential LINE-1 regulation in pluripotent stem cells of humans and other great apes
title Differential LINE-1 regulation in pluripotent stem cells of humans and other great apes
title_full Differential LINE-1 regulation in pluripotent stem cells of humans and other great apes
title_fullStr Differential LINE-1 regulation in pluripotent stem cells of humans and other great apes
title_full_unstemmed Differential LINE-1 regulation in pluripotent stem cells of humans and other great apes
title_short Differential LINE-1 regulation in pluripotent stem cells of humans and other great apes
title_sort differential line-1 regulation in pluripotent stem cells of humans and other great apes
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4064720/
https://www.ncbi.nlm.nih.gov/pubmed/24153179
http://dx.doi.org/10.1038/nature12686
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