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GATA6 Is a Crucial Regulator of Shh in the Limb Bud
In the limb bud, patterning along the anterior-posterior (A-P) axis is controlled by Sonic Hedgehog (Shh), a signaling molecule secreted by the “Zone of Polarizing Activity”, an organizer tissue located in the posterior margin of the limb bud. We have found that the transcription factors GATA4 and G...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3886911/ https://www.ncbi.nlm.nih.gov/pubmed/24415953 http://dx.doi.org/10.1371/journal.pgen.1004072 |
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author | Kozhemyakina, Elena Ionescu, Andreia Lassar, Andrew B. |
author_facet | Kozhemyakina, Elena Ionescu, Andreia Lassar, Andrew B. |
author_sort | Kozhemyakina, Elena |
collection | PubMed |
description | In the limb bud, patterning along the anterior-posterior (A-P) axis is controlled by Sonic Hedgehog (Shh), a signaling molecule secreted by the “Zone of Polarizing Activity”, an organizer tissue located in the posterior margin of the limb bud. We have found that the transcription factors GATA4 and GATA6, which are key regulators of cell identity, are expressed in an anterior to posterior gradient in the early limb bud, raising the possibility that GATA transcription factors may play an additional role in patterning this tissue. While both GATA4 and GATA6 are expressed in an A-P gradient in the forelimb buds, the hindlimb buds principally express GATA6 in an A-P gradient. Thus, to specifically examine the role of GATA6 in limb patterning we generated Prx1-Cre; GATA6(fl/fl) mice, which conditionally delete GATA6 from their developing limb buds. We found that these animals display ectopic expression of both Shh and its transcriptional targets specifically in the anterior mesenchyme of the hindlimb buds. Loss of GATA6 in the developing limbs results in the formation of preaxial polydactyly in the hindlimbs. Conversely, forced expression of GATA6 throughout the limb bud represses expression of Shh and results in hypomorphic limbs. We have found that GATA6 can bind to chromatin (isolated from limb buds) encoding either Shh or Gli1 regulatory elements that drive expression of these genes in this tissue, and demonstrated that GATA6 works synergistically with FOG co-factors to repress expression of luciferase reporters driven by these sequences. Most significantly, we have found that conditional loss of Shh in limb buds lacking GATA6 prevents development of hindlimb polydactyly in these compound mutant embryos, indicating that GATA6 expression in the anterior region of the limb bud blocks hindlimb polydactyly by repressing ectopic expression of Shh. |
format | Online Article Text |
id | pubmed-3886911 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-38869112014-01-10 GATA6 Is a Crucial Regulator of Shh in the Limb Bud Kozhemyakina, Elena Ionescu, Andreia Lassar, Andrew B. PLoS Genet Research Article In the limb bud, patterning along the anterior-posterior (A-P) axis is controlled by Sonic Hedgehog (Shh), a signaling molecule secreted by the “Zone of Polarizing Activity”, an organizer tissue located in the posterior margin of the limb bud. We have found that the transcription factors GATA4 and GATA6, which are key regulators of cell identity, are expressed in an anterior to posterior gradient in the early limb bud, raising the possibility that GATA transcription factors may play an additional role in patterning this tissue. While both GATA4 and GATA6 are expressed in an A-P gradient in the forelimb buds, the hindlimb buds principally express GATA6 in an A-P gradient. Thus, to specifically examine the role of GATA6 in limb patterning we generated Prx1-Cre; GATA6(fl/fl) mice, which conditionally delete GATA6 from their developing limb buds. We found that these animals display ectopic expression of both Shh and its transcriptional targets specifically in the anterior mesenchyme of the hindlimb buds. Loss of GATA6 in the developing limbs results in the formation of preaxial polydactyly in the hindlimbs. Conversely, forced expression of GATA6 throughout the limb bud represses expression of Shh and results in hypomorphic limbs. We have found that GATA6 can bind to chromatin (isolated from limb buds) encoding either Shh or Gli1 regulatory elements that drive expression of these genes in this tissue, and demonstrated that GATA6 works synergistically with FOG co-factors to repress expression of luciferase reporters driven by these sequences. Most significantly, we have found that conditional loss of Shh in limb buds lacking GATA6 prevents development of hindlimb polydactyly in these compound mutant embryos, indicating that GATA6 expression in the anterior region of the limb bud blocks hindlimb polydactyly by repressing ectopic expression of Shh. Public Library of Science 2014-01-09 /pmc/articles/PMC3886911/ /pubmed/24415953 http://dx.doi.org/10.1371/journal.pgen.1004072 Text en © 2014 Kozhemyakina et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Kozhemyakina, Elena Ionescu, Andreia Lassar, Andrew B. GATA6 Is a Crucial Regulator of Shh in the Limb Bud |
title | GATA6 Is a Crucial Regulator of Shh in the Limb Bud |
title_full | GATA6 Is a Crucial Regulator of Shh in the Limb Bud |
title_fullStr | GATA6 Is a Crucial Regulator of Shh in the Limb Bud |
title_full_unstemmed | GATA6 Is a Crucial Regulator of Shh in the Limb Bud |
title_short | GATA6 Is a Crucial Regulator of Shh in the Limb Bud |
title_sort | gata6 is a crucial regulator of shh in the limb bud |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3886911/ https://www.ncbi.nlm.nih.gov/pubmed/24415953 http://dx.doi.org/10.1371/journal.pgen.1004072 |
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