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A catalog of Xenopus tropicalis transcription factors and their regional expression in the early gastrula stage embryo
Gene regulatory networks (GRNs) involve highly combinatorial interactions between transcription factors and short sequence motifs in cis-regulatory modules of target genes to control cellular phenotypes. The GRNs specifying most cell types are largely unknown and are the subject of wide interest. A...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5596316/ https://www.ncbi.nlm.nih.gov/pubmed/27475627 http://dx.doi.org/10.1016/j.ydbio.2016.07.002 |
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author | Blitz, Ira L. Paraiso, Kitt D. Patrushev, Ilya Chiu, William T.Y. Cho, Ken W.Y. Gilchrist, Michael J. |
author_facet | Blitz, Ira L. Paraiso, Kitt D. Patrushev, Ilya Chiu, William T.Y. Cho, Ken W.Y. Gilchrist, Michael J. |
author_sort | Blitz, Ira L. |
collection | PubMed |
description | Gene regulatory networks (GRNs) involve highly combinatorial interactions between transcription factors and short sequence motifs in cis-regulatory modules of target genes to control cellular phenotypes. The GRNs specifying most cell types are largely unknown and are the subject of wide interest. A catalog of transcription factors is a valuable tool toward obtaining a deeper understanding of the role of these critical effectors in any biological setting. Here we present a comprehensive catalog of the transcription factors for the diploid frog Xenopus tropicalis. We identify 1235 genes encoding DNA-binding transcription factors, comparable to the numbers found in typical mammalian species. In detail, the repertoire of X. tropicalis transcription factor genes is nearly identical to human and mouse, with the exception of zinc finger family members, and a small number of species/lineage-specific gene duplications and losses relative to the mammalian repertoires. We applied this resource to the identification of transcription factors differentially expressed in the early gastrula stage embryo. We find transcription factor enrichment in Spemann's organizer, the ventral mesoderm, ectoderm and endoderm, and report 218 TFs that show regionalized expression patterns at this stage. Many of these have not been previously reported as expressed in the early embryo, suggesting thus far unappreciated roles for many transcription factors in the GRNs regulating early development. We expect our transcription factor catalog will facilitate myriad studies using Xenopus as a model system to understand basic biology and human disease. |
format | Online Article Text |
id | pubmed-5596316 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
record_format | MEDLINE/PubMed |
spelling | pubmed-55963162018-01-18 A catalog of Xenopus tropicalis transcription factors and their regional expression in the early gastrula stage embryo Blitz, Ira L. Paraiso, Kitt D. Patrushev, Ilya Chiu, William T.Y. Cho, Ken W.Y. Gilchrist, Michael J. Dev Biol Article Gene regulatory networks (GRNs) involve highly combinatorial interactions between transcription factors and short sequence motifs in cis-regulatory modules of target genes to control cellular phenotypes. The GRNs specifying most cell types are largely unknown and are the subject of wide interest. A catalog of transcription factors is a valuable tool toward obtaining a deeper understanding of the role of these critical effectors in any biological setting. Here we present a comprehensive catalog of the transcription factors for the diploid frog Xenopus tropicalis. We identify 1235 genes encoding DNA-binding transcription factors, comparable to the numbers found in typical mammalian species. In detail, the repertoire of X. tropicalis transcription factor genes is nearly identical to human and mouse, with the exception of zinc finger family members, and a small number of species/lineage-specific gene duplications and losses relative to the mammalian repertoires. We applied this resource to the identification of transcription factors differentially expressed in the early gastrula stage embryo. We find transcription factor enrichment in Spemann's organizer, the ventral mesoderm, ectoderm and endoderm, and report 218 TFs that show regionalized expression patterns at this stage. Many of these have not been previously reported as expressed in the early embryo, suggesting thus far unappreciated roles for many transcription factors in the GRNs regulating early development. We expect our transcription factor catalog will facilitate myriad studies using Xenopus as a model system to understand basic biology and human disease. 2016-07-28 2017-06-15 /pmc/articles/PMC5596316/ /pubmed/27475627 http://dx.doi.org/10.1016/j.ydbio.2016.07.002 Text en This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Blitz, Ira L. Paraiso, Kitt D. Patrushev, Ilya Chiu, William T.Y. Cho, Ken W.Y. Gilchrist, Michael J. A catalog of Xenopus tropicalis transcription factors and their regional expression in the early gastrula stage embryo |
title | A catalog of Xenopus tropicalis transcription factors and their regional expression in the early gastrula stage embryo |
title_full | A catalog of Xenopus tropicalis transcription factors and their regional expression in the early gastrula stage embryo |
title_fullStr | A catalog of Xenopus tropicalis transcription factors and their regional expression in the early gastrula stage embryo |
title_full_unstemmed | A catalog of Xenopus tropicalis transcription factors and their regional expression in the early gastrula stage embryo |
title_short | A catalog of Xenopus tropicalis transcription factors and their regional expression in the early gastrula stage embryo |
title_sort | catalog of xenopus tropicalis transcription factors and their regional expression in the early gastrula stage embryo |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5596316/ https://www.ncbi.nlm.nih.gov/pubmed/27475627 http://dx.doi.org/10.1016/j.ydbio.2016.07.002 |
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