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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 recently studied in great apes, however, the diversity of splicing variants rem...

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Autores principales: Tomaszkiewicz, Marta, Sahlin, Kristoffer, Medvedev, Paul, Makova, Kateryna D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cold Spring Harbor Laboratory 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10054944/
https://www.ncbi.nlm.nih.gov/pubmed/36993458
http://dx.doi.org/10.1101/2023.03.02.530874
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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 recently 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 dataset resulted in several findings. First, we uncovered a high diversity of YAG transcripts across great apes. Second, we observed evolutionarily conserved alternative splicing patterns for most YAG families except for BPY2 and PRY. Our results suggest that BPY2 transcripts and predicted proteins in several great ape species (bonobo and the two orangutans) have independent evolutionary origins and are not homologous to human reference transcripts and proteins. In contrast, our results suggest that the PRY gene family, having the highest representation of transcripts without open reading frames, has been undergoing pseudogenization. Third, even though we have identified many species-specific protein-coding YAG transcripts, we have not detected any signatures of positive selection. Overall, our work illuminates the YAG isoform landscape and its evolutionary history, 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-100549442023-03-30 Transcript Isoform Diversity of Ampliconic Genes on the Y Chromosome of Great Apes Tomaszkiewicz, Marta Sahlin, Kristoffer Medvedev, Paul Makova, Kateryna D. bioRxiv 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 recently 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 dataset resulted in several findings. First, we uncovered a high diversity of YAG transcripts across great apes. Second, we observed evolutionarily conserved alternative splicing patterns for most YAG families except for BPY2 and PRY. Our results suggest that BPY2 transcripts and predicted proteins in several great ape species (bonobo and the two orangutans) have independent evolutionary origins and are not homologous to human reference transcripts and proteins. In contrast, our results suggest that the PRY gene family, having the highest representation of transcripts without open reading frames, has been undergoing pseudogenization. Third, even though we have identified many species-specific protein-coding YAG transcripts, we have not detected any signatures of positive selection. Overall, our work illuminates the YAG isoform landscape and its evolutionary history, and provides a genomic resource for future functional studies focusing on infertility phenotypes in humans and critically endangered great apes. Cold Spring Harbor Laboratory 2023-03-18 /pmc/articles/PMC10054944/ /pubmed/36993458 http://dx.doi.org/10.1101/2023.03.02.530874 Text en https://creativecommons.org/licenses/by-nc-nd/4.0/This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which allows reusers to copy and distribute the material in any medium or format in unadapted form only, for noncommercial purposes only, and only so long as attribution is given to the creator.
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/PMC10054944/
https://www.ncbi.nlm.nih.gov/pubmed/36993458
http://dx.doi.org/10.1101/2023.03.02.530874
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