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PADI6: What we know about the elusive fifth member of the peptidyl arginine deiminase family
Peptidyl arginine deiminase 6 (PADI6) is a maternal factor that is vital for early embryonic development. Deletion and mutations of its encoding gene in female mice or women lead to early embryonic developmental arrest, female infertility, maternal imprinting defects and hyperproliferation of the tr...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10542454/ https://www.ncbi.nlm.nih.gov/pubmed/37778376 http://dx.doi.org/10.1098/rstb.2022.0242 |
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author | Williams, Jack P. C. Walport, Louise J. |
author_facet | Williams, Jack P. C. Walport, Louise J. |
author_sort | Williams, Jack P. C. |
collection | PubMed |
description | Peptidyl arginine deiminase 6 (PADI6) is a maternal factor that is vital for early embryonic development. Deletion and mutations of its encoding gene in female mice or women lead to early embryonic developmental arrest, female infertility, maternal imprinting defects and hyperproliferation of the trophoblast. PADI6 is the fifth and least well-characterized member of the peptidyl arginine deiminases (PADIs), which catalyse the post-translational conversion of arginine to citrulline. It is less conserved than the other PADIs, and currently has no reported catalytic activity. While there are many suggested functions of PADI6 in the early mouse embryo, including in embryonic genome activation, cytoplasmic lattice formation, maternal mRNA and ribosome regulation, and organelle distribution, the molecular mechanisms of its function remain unknown. In this review, we discuss what is known about the function of PADI6 and highlight key outstanding questions that must be answered if we are to understand the crucial role it plays in early embryo development and female fertility. This article is part of the Theo Murphy meeting issue ‘The virtues and vices of protein citrullination’. |
format | Online Article Text |
id | pubmed-10542454 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | The Royal Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-105424542023-10-03 PADI6: What we know about the elusive fifth member of the peptidyl arginine deiminase family Williams, Jack P. C. Walport, Louise J. Philos Trans R Soc Lond B Biol Sci Articles Peptidyl arginine deiminase 6 (PADI6) is a maternal factor that is vital for early embryonic development. Deletion and mutations of its encoding gene in female mice or women lead to early embryonic developmental arrest, female infertility, maternal imprinting defects and hyperproliferation of the trophoblast. PADI6 is the fifth and least well-characterized member of the peptidyl arginine deiminases (PADIs), which catalyse the post-translational conversion of arginine to citrulline. It is less conserved than the other PADIs, and currently has no reported catalytic activity. While there are many suggested functions of PADI6 in the early mouse embryo, including in embryonic genome activation, cytoplasmic lattice formation, maternal mRNA and ribosome regulation, and organelle distribution, the molecular mechanisms of its function remain unknown. In this review, we discuss what is known about the function of PADI6 and highlight key outstanding questions that must be answered if we are to understand the crucial role it plays in early embryo development and female fertility. This article is part of the Theo Murphy meeting issue ‘The virtues and vices of protein citrullination’. The Royal Society 2023-11-20 2023-10-02 /pmc/articles/PMC10542454/ /pubmed/37778376 http://dx.doi.org/10.1098/rstb.2022.0242 Text en © 2023 The Authors. https://creativecommons.org/licenses/by/4.0/Published by the Royal Society under the terms of the Creative Commons Attribution License http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, provided the original author and source are credited. |
spellingShingle | Articles Williams, Jack P. C. Walport, Louise J. PADI6: What we know about the elusive fifth member of the peptidyl arginine deiminase family |
title | PADI6: What we know about the elusive fifth member of the peptidyl arginine deiminase family |
title_full | PADI6: What we know about the elusive fifth member of the peptidyl arginine deiminase family |
title_fullStr | PADI6: What we know about the elusive fifth member of the peptidyl arginine deiminase family |
title_full_unstemmed | PADI6: What we know about the elusive fifth member of the peptidyl arginine deiminase family |
title_short | PADI6: What we know about the elusive fifth member of the peptidyl arginine deiminase family |
title_sort | padi6: what we know about the elusive fifth member of the peptidyl arginine deiminase family |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10542454/ https://www.ncbi.nlm.nih.gov/pubmed/37778376 http://dx.doi.org/10.1098/rstb.2022.0242 |
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