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Identification and functional characterization of novel transcriptional enhancers involved in regulating human GLI3 expression during early development
The zinc‐finger transcription factor GLI3 acts as a primary transducer of Sonic hedgehog (Shh) signaling in a context‐dependent combinatorial fashion. GLI3 participates in the patterning and growth of many organs, including the central nervous system (CNS) and limbs. Previously, we reported a subset...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4609622/ https://www.ncbi.nlm.nih.gov/pubmed/26464005 http://dx.doi.org/10.1111/dgd.12239 |
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author | Anwar, Saneela Minhas, Rashid Ali, Shahid Lambert, Nicholas Kawakami, Yasuhiko Elgar, Greg Azam, Syed Sikandar Abbasi, Amir Ali |
author_facet | Anwar, Saneela Minhas, Rashid Ali, Shahid Lambert, Nicholas Kawakami, Yasuhiko Elgar, Greg Azam, Syed Sikandar Abbasi, Amir Ali |
author_sort | Anwar, Saneela |
collection | PubMed |
description | The zinc‐finger transcription factor GLI3 acts as a primary transducer of Sonic hedgehog (Shh) signaling in a context‐dependent combinatorial fashion. GLI3 participates in the patterning and growth of many organs, including the central nervous system (CNS) and limbs. Previously, we reported a subset of human intronic cis‐regulators controlling many known aspects of endogenous Gli3 expression in mouse and zebrafish. Here we demonstrate in a transgenic zebrafish assay the potential of two novel tetrapod‐teleost conserved non‐coding elements (CNEs) docking within GLI3 intronic intervals (intron 3 and 4) to induce reporter gene expression at known sites of endogenous Gli3 transcription in embryonic domains such as the central nervous system (CNS) and limbs. Interestingly, the cell culture based assays reveal harmony with the context dependent dual nature of intra‐GLI3 conserved elements. Furthermore, a transgenic zebrafish assay of previously reported limb‐specific GLI3 transcriptional enhancers (previously tested in mice and chicken limb buds) induced reporter gene expression in zebrafish blood precursor cells and notochord instead of fin. These results demonstrate that the appendage‐specific activity of a subset of GLI3‐associated enhancers might be a tetrapod innovation. Taken together with our recent data, these results suggest that during the course of vertebrate evolution Gli3 expression control acquired a complex cis‐regulatory landscape for spatiotemporal patterning of CNS and limbs. Comparative data from fish and mice suggest that the functional aspects of a subset of these cis‐regulators have diverged significantly between these two lineages. |
format | Online Article Text |
id | pubmed-4609622 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-46096222016-04-15 Identification and functional characterization of novel transcriptional enhancers involved in regulating human GLI3 expression during early development Anwar, Saneela Minhas, Rashid Ali, Shahid Lambert, Nicholas Kawakami, Yasuhiko Elgar, Greg Azam, Syed Sikandar Abbasi, Amir Ali Dev Growth Differ Original Articles The zinc‐finger transcription factor GLI3 acts as a primary transducer of Sonic hedgehog (Shh) signaling in a context‐dependent combinatorial fashion. GLI3 participates in the patterning and growth of many organs, including the central nervous system (CNS) and limbs. Previously, we reported a subset of human intronic cis‐regulators controlling many known aspects of endogenous Gli3 expression in mouse and zebrafish. Here we demonstrate in a transgenic zebrafish assay the potential of two novel tetrapod‐teleost conserved non‐coding elements (CNEs) docking within GLI3 intronic intervals (intron 3 and 4) to induce reporter gene expression at known sites of endogenous Gli3 transcription in embryonic domains such as the central nervous system (CNS) and limbs. Interestingly, the cell culture based assays reveal harmony with the context dependent dual nature of intra‐GLI3 conserved elements. Furthermore, a transgenic zebrafish assay of previously reported limb‐specific GLI3 transcriptional enhancers (previously tested in mice and chicken limb buds) induced reporter gene expression in zebrafish blood precursor cells and notochord instead of fin. These results demonstrate that the appendage‐specific activity of a subset of GLI3‐associated enhancers might be a tetrapod innovation. Taken together with our recent data, these results suggest that during the course of vertebrate evolution Gli3 expression control acquired a complex cis‐regulatory landscape for spatiotemporal patterning of CNS and limbs. Comparative data from fish and mice suggest that the functional aspects of a subset of these cis‐regulators have diverged significantly between these two lineages. John Wiley and Sons Inc. 2015-10-14 2015-10 /pmc/articles/PMC4609622/ /pubmed/26464005 http://dx.doi.org/10.1111/dgd.12239 Text en © 2015 The Authors Development, Growth & Differentiation published by Wiley Publishing Asia Pty Ltd on behalf of Japanese Society of Developmental Biologists This is an open access article under the terms of the Creative Commons Attribution (http://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Articles Anwar, Saneela Minhas, Rashid Ali, Shahid Lambert, Nicholas Kawakami, Yasuhiko Elgar, Greg Azam, Syed Sikandar Abbasi, Amir Ali Identification and functional characterization of novel transcriptional enhancers involved in regulating human GLI3 expression during early development |
title | Identification and functional characterization of novel transcriptional enhancers involved in regulating human GLI3 expression during early development |
title_full | Identification and functional characterization of novel transcriptional enhancers involved in regulating human GLI3 expression during early development |
title_fullStr | Identification and functional characterization of novel transcriptional enhancers involved in regulating human GLI3 expression during early development |
title_full_unstemmed | Identification and functional characterization of novel transcriptional enhancers involved in regulating human GLI3 expression during early development |
title_short | Identification and functional characterization of novel transcriptional enhancers involved in regulating human GLI3 expression during early development |
title_sort | identification and functional characterization of novel transcriptional enhancers involved in regulating human gli3 expression during early development |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4609622/ https://www.ncbi.nlm.nih.gov/pubmed/26464005 http://dx.doi.org/10.1111/dgd.12239 |
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