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Phenotypic variability in two female siblings with oocyte maturation arrest due to a TUBB8 variant
Tubulin beta-8 (TUBB8) is expressed exclusively in the oocyte and early embryo, encoding a beta-tubulin polypeptide that participates in the assembly of microtubules. TUBB8 was first attributed to being responsible for oocyte MI arrest. Further studies have demonstrated that patients with different...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10614405/ https://www.ncbi.nlm.nih.gov/pubmed/37904145 http://dx.doi.org/10.1186/s12920-023-01712-7 |
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author | Dou, Qian Xu, HongEn Ma, LiYing Tan, Li Tang, WenXue |
author_facet | Dou, Qian Xu, HongEn Ma, LiYing Tan, Li Tang, WenXue |
author_sort | Dou, Qian |
collection | PubMed |
description | Tubulin beta-8 (TUBB8) is expressed exclusively in the oocyte and early embryo, encoding a beta-tubulin polypeptide that participates in the assembly of microtubules. TUBB8 was first attributed to being responsible for oocyte MI arrest. Further studies have demonstrated that patients with different pathogenic variants have variable phenotypes. We report a TUBB8 variant (c.10 A > C) in two siblings who presented different clinical features of primary infertility. The younger sister showed severe oocyte maturation arrest with abnormal morphology, whereas a few mature oocytes and zygotes could be retrieved from the older sister, but no embryo was available for transfer. This variant was previously reported without in vitro functional assays. In the present study, RT‒qPCR and western blot analyses revealed that c.10 A > C reduces TUBB8 mRNA and protein levels; however, immunofluorescence demonstrated that this variant does not change the localization of the protein. These findings confirm the pathogenicity of the c.10 A > C variant and support the relationship between the variant and phenotype in the patients. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12920-023-01712-7. |
format | Online Article Text |
id | pubmed-10614405 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-106144052023-10-31 Phenotypic variability in two female siblings with oocyte maturation arrest due to a TUBB8 variant Dou, Qian Xu, HongEn Ma, LiYing Tan, Li Tang, WenXue BMC Med Genomics Research Tubulin beta-8 (TUBB8) is expressed exclusively in the oocyte and early embryo, encoding a beta-tubulin polypeptide that participates in the assembly of microtubules. TUBB8 was first attributed to being responsible for oocyte MI arrest. Further studies have demonstrated that patients with different pathogenic variants have variable phenotypes. We report a TUBB8 variant (c.10 A > C) in two siblings who presented different clinical features of primary infertility. The younger sister showed severe oocyte maturation arrest with abnormal morphology, whereas a few mature oocytes and zygotes could be retrieved from the older sister, but no embryo was available for transfer. This variant was previously reported without in vitro functional assays. In the present study, RT‒qPCR and western blot analyses revealed that c.10 A > C reduces TUBB8 mRNA and protein levels; however, immunofluorescence demonstrated that this variant does not change the localization of the protein. These findings confirm the pathogenicity of the c.10 A > C variant and support the relationship between the variant and phenotype in the patients. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12920-023-01712-7. BioMed Central 2023-10-30 /pmc/articles/PMC10614405/ /pubmed/37904145 http://dx.doi.org/10.1186/s12920-023-01712-7 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Dou, Qian Xu, HongEn Ma, LiYing Tan, Li Tang, WenXue Phenotypic variability in two female siblings with oocyte maturation arrest due to a TUBB8 variant |
title | Phenotypic variability in two female siblings with oocyte maturation arrest due to a TUBB8 variant |
title_full | Phenotypic variability in two female siblings with oocyte maturation arrest due to a TUBB8 variant |
title_fullStr | Phenotypic variability in two female siblings with oocyte maturation arrest due to a TUBB8 variant |
title_full_unstemmed | Phenotypic variability in two female siblings with oocyte maturation arrest due to a TUBB8 variant |
title_short | Phenotypic variability in two female siblings with oocyte maturation arrest due to a TUBB8 variant |
title_sort | phenotypic variability in two female siblings with oocyte maturation arrest due to a tubb8 variant |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10614405/ https://www.ncbi.nlm.nih.gov/pubmed/37904145 http://dx.doi.org/10.1186/s12920-023-01712-7 |
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