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Common ancestry of heterodimerizing TALE homeobox transcription factors across Metazoa and Archaeplastida
BACKGROUND: Complex multicellularity requires elaborate developmental mechanisms, often based on the versatility of heterodimeric transcription factor (TF) interactions. Homeobox TFs in the TALE superclass are deeply embedded in the gene regulatory networks that orchestrate embryogenesis. Knotted-li...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6219170/ https://www.ncbi.nlm.nih.gov/pubmed/30396330 http://dx.doi.org/10.1186/s12915-018-0605-5 |
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author | Joo, Sunjoo Wang, Ming Hsiu Lui, Gary Lee, Jenny Barnas, Andrew Kim, Eunsoo Sudek, Sebastian Worden, Alexandra Z. Lee, Jae-Hyeok |
author_facet | Joo, Sunjoo Wang, Ming Hsiu Lui, Gary Lee, Jenny Barnas, Andrew Kim, Eunsoo Sudek, Sebastian Worden, Alexandra Z. Lee, Jae-Hyeok |
author_sort | Joo, Sunjoo |
collection | PubMed |
description | BACKGROUND: Complex multicellularity requires elaborate developmental mechanisms, often based on the versatility of heterodimeric transcription factor (TF) interactions. Homeobox TFs in the TALE superclass are deeply embedded in the gene regulatory networks that orchestrate embryogenesis. Knotted-like homeobox (KNOX) TFs, homologous to animal MEIS, have been found to drive the haploid-to-diploid transition in both unicellular green algae and land plants via heterodimerization with other TALE superclass TFs, demonstrating remarkable functional conservation of a developmental TF across lineages that diverged one billion years ago. Here, we sought to delineate whether TALE-TALE heterodimerization is ancestral to eukaryotes. RESULTS: We analyzed TALE endowment in the algal radiations of Archaeplastida, ancestral to land plants. Homeodomain phylogeny and bioinformatics analysis partitioned TALEs into two broad groups, KNOX and non-KNOX. Each group shares previously defined heterodimerization domains, plant KNOX-homology in the KNOX group and animal PBC-homology in the non-KNOX group, indicating their deep ancestry. Protein-protein interaction experiments showed that the TALEs in the two groups all participated in heterodimerization. CONCLUSIONS: Our study indicates that the TF dyads consisting of KNOX/MEIS and PBC-containing TALEs must have evolved early in eukaryotic evolution. Based on our results, we hypothesize that in early eukaryotes, the TALE heterodimeric configuration provided transcription-on switches via dimerization-dependent subcellular localization, ensuring execution of the haploid-to-diploid transition only when the gamete fusion is correctly executed between appropriate partner gametes. The TALE switch then diversified in the several lineages that engage in a complex multicellular organization. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12915-018-0605-5) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-6219170 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-62191702018-11-16 Common ancestry of heterodimerizing TALE homeobox transcription factors across Metazoa and Archaeplastida Joo, Sunjoo Wang, Ming Hsiu Lui, Gary Lee, Jenny Barnas, Andrew Kim, Eunsoo Sudek, Sebastian Worden, Alexandra Z. Lee, Jae-Hyeok BMC Biol Research Article BACKGROUND: Complex multicellularity requires elaborate developmental mechanisms, often based on the versatility of heterodimeric transcription factor (TF) interactions. Homeobox TFs in the TALE superclass are deeply embedded in the gene regulatory networks that orchestrate embryogenesis. Knotted-like homeobox (KNOX) TFs, homologous to animal MEIS, have been found to drive the haploid-to-diploid transition in both unicellular green algae and land plants via heterodimerization with other TALE superclass TFs, demonstrating remarkable functional conservation of a developmental TF across lineages that diverged one billion years ago. Here, we sought to delineate whether TALE-TALE heterodimerization is ancestral to eukaryotes. RESULTS: We analyzed TALE endowment in the algal radiations of Archaeplastida, ancestral to land plants. Homeodomain phylogeny and bioinformatics analysis partitioned TALEs into two broad groups, KNOX and non-KNOX. Each group shares previously defined heterodimerization domains, plant KNOX-homology in the KNOX group and animal PBC-homology in the non-KNOX group, indicating their deep ancestry. Protein-protein interaction experiments showed that the TALEs in the two groups all participated in heterodimerization. CONCLUSIONS: Our study indicates that the TF dyads consisting of KNOX/MEIS and PBC-containing TALEs must have evolved early in eukaryotic evolution. Based on our results, we hypothesize that in early eukaryotes, the TALE heterodimeric configuration provided transcription-on switches via dimerization-dependent subcellular localization, ensuring execution of the haploid-to-diploid transition only when the gamete fusion is correctly executed between appropriate partner gametes. The TALE switch then diversified in the several lineages that engage in a complex multicellular organization. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12915-018-0605-5) contains supplementary material, which is available to authorized users. BioMed Central 2018-11-05 /pmc/articles/PMC6219170/ /pubmed/30396330 http://dx.doi.org/10.1186/s12915-018-0605-5 Text en © The Author(s). 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Joo, Sunjoo Wang, Ming Hsiu Lui, Gary Lee, Jenny Barnas, Andrew Kim, Eunsoo Sudek, Sebastian Worden, Alexandra Z. Lee, Jae-Hyeok Common ancestry of heterodimerizing TALE homeobox transcription factors across Metazoa and Archaeplastida |
title | Common ancestry of heterodimerizing TALE homeobox transcription factors across Metazoa and Archaeplastida |
title_full | Common ancestry of heterodimerizing TALE homeobox transcription factors across Metazoa and Archaeplastida |
title_fullStr | Common ancestry of heterodimerizing TALE homeobox transcription factors across Metazoa and Archaeplastida |
title_full_unstemmed | Common ancestry of heterodimerizing TALE homeobox transcription factors across Metazoa and Archaeplastida |
title_short | Common ancestry of heterodimerizing TALE homeobox transcription factors across Metazoa and Archaeplastida |
title_sort | common ancestry of heterodimerizing tale homeobox transcription factors across metazoa and archaeplastida |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6219170/ https://www.ncbi.nlm.nih.gov/pubmed/30396330 http://dx.doi.org/10.1186/s12915-018-0605-5 |
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