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Transcript Isoform Diversity of Ampliconic Genes on the Y Chromosome of Great Apes

Y chromosomal ampliconic genes (YAGs) are important for male fertility, as they encode proteins functioning in spermatogenesis. The variation in copy number and expression levels of these multicopy gene families has been studied in great apes; however, the diversity of splicing variants remains unex...

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Autores principales: Tomaszkiewicz, Marta, Sahlin, Kristoffer, Medvedev, Paul, Makova, Kateryna D
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10673640/
https://www.ncbi.nlm.nih.gov/pubmed/37967251
http://dx.doi.org/10.1093/gbe/evad205
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author Tomaszkiewicz, Marta
Sahlin, Kristoffer
Medvedev, Paul
Makova, Kateryna D
author_facet Tomaszkiewicz, Marta
Sahlin, Kristoffer
Medvedev, Paul
Makova, Kateryna D
author_sort Tomaszkiewicz, Marta
collection PubMed
description Y chromosomal ampliconic genes (YAGs) are important for male fertility, as they encode proteins functioning in spermatogenesis. The variation in copy number and expression levels of these multicopy gene families has been studied in great apes; however, the diversity of splicing variants remains unexplored. Here, we deciphered the sequences of polyadenylated transcripts of all nine YAG families (BPY2, CDY, DAZ, HSFY, PRY, RBMY, TSPY, VCY, and XKRY) from testis samples of six great ape species (human, chimpanzee, bonobo, gorilla, Bornean orangutan, and Sumatran orangutan). To achieve this, we enriched YAG transcripts with capture probe hybridization and sequenced them with long (Pacific Biosciences) reads. Our analysis of this data set resulted in several findings. First, we observed evolutionarily conserved alternative splicing patterns for most YAG families except for BPY2 and PRY. Second, our results suggest that BPY2 transcripts and proteins originate from separate genomic regions in bonobo versus human, which is possibly facilitated by acquiring new promoters. Third, our analysis indicates that the PRY gene family, having the highest representation of noncoding transcripts, has been undergoing pseudogenization. Fourth, we have not detected signatures of selection in the five YAG families shared among great apes, even though we identified many species-specific protein-coding transcripts. Fifth, we predicted consensus disorder regions across most gene families and species, which could be used for future investigations of male infertility. Overall, our work illuminates the YAG isoform landscape and provides a genomic resource for future functional studies focusing on infertility phenotypes in humans and critically endangered great apes.
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spelling pubmed-106736402023-11-15 Transcript Isoform Diversity of Ampliconic Genes on the Y Chromosome of Great Apes Tomaszkiewicz, Marta Sahlin, Kristoffer Medvedev, Paul Makova, Kateryna D Genome Biol Evol Article Y chromosomal ampliconic genes (YAGs) are important for male fertility, as they encode proteins functioning in spermatogenesis. The variation in copy number and expression levels of these multicopy gene families has been studied in great apes; however, the diversity of splicing variants remains unexplored. Here, we deciphered the sequences of polyadenylated transcripts of all nine YAG families (BPY2, CDY, DAZ, HSFY, PRY, RBMY, TSPY, VCY, and XKRY) from testis samples of six great ape species (human, chimpanzee, bonobo, gorilla, Bornean orangutan, and Sumatran orangutan). To achieve this, we enriched YAG transcripts with capture probe hybridization and sequenced them with long (Pacific Biosciences) reads. Our analysis of this data set resulted in several findings. First, we observed evolutionarily conserved alternative splicing patterns for most YAG families except for BPY2 and PRY. Second, our results suggest that BPY2 transcripts and proteins originate from separate genomic regions in bonobo versus human, which is possibly facilitated by acquiring new promoters. Third, our analysis indicates that the PRY gene family, having the highest representation of noncoding transcripts, has been undergoing pseudogenization. Fourth, we have not detected signatures of selection in the five YAG families shared among great apes, even though we identified many species-specific protein-coding transcripts. Fifth, we predicted consensus disorder regions across most gene families and species, which could be used for future investigations of male infertility. Overall, our work illuminates the YAG isoform landscape and provides a genomic resource for future functional studies focusing on infertility phenotypes in humans and critically endangered great apes. Oxford University Press 2023-11-15 /pmc/articles/PMC10673640/ /pubmed/37967251 http://dx.doi.org/10.1093/gbe/evad205 Text en © The Author(s) 2023. Published by Oxford University Press on behalf of Society for Molecular Biology and Evolution. https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License (https://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Article
Tomaszkiewicz, Marta
Sahlin, Kristoffer
Medvedev, Paul
Makova, Kateryna D
Transcript Isoform Diversity of Ampliconic Genes on the Y Chromosome of Great Apes
title Transcript Isoform Diversity of Ampliconic Genes on the Y Chromosome of Great Apes
title_full Transcript Isoform Diversity of Ampliconic Genes on the Y Chromosome of Great Apes
title_fullStr Transcript Isoform Diversity of Ampliconic Genes on the Y Chromosome of Great Apes
title_full_unstemmed Transcript Isoform Diversity of Ampliconic Genes on the Y Chromosome of Great Apes
title_short Transcript Isoform Diversity of Ampliconic Genes on the Y Chromosome of Great Apes
title_sort transcript isoform diversity of ampliconic genes on the y chromosome of great apes
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10673640/
https://www.ncbi.nlm.nih.gov/pubmed/37967251
http://dx.doi.org/10.1093/gbe/evad205
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