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Architectural groups of a subtelomeric gene family evolve along distinct paths in Candida albicans

Subtelomeres are dynamic genomic regions shaped by elevated rates of recombination, mutation, and gene birth/death. These processes contribute to formation of lineage-specific gene family expansions that commonly occupy subtelomeres across eukaryotes. Investigating the evolution of subtelomeric gene...

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Autores principales: Dunn, Matthew J, Shazib, Shahed U A, Simonton, Emily, Slot, Jason C, Anderson, Matthew Z
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9713401/
https://www.ncbi.nlm.nih.gov/pubmed/36269198
http://dx.doi.org/10.1093/g3journal/jkac283
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author Dunn, Matthew J
Shazib, Shahed U A
Simonton, Emily
Slot, Jason C
Anderson, Matthew Z
author_facet Dunn, Matthew J
Shazib, Shahed U A
Simonton, Emily
Slot, Jason C
Anderson, Matthew Z
author_sort Dunn, Matthew J
collection PubMed
description Subtelomeres are dynamic genomic regions shaped by elevated rates of recombination, mutation, and gene birth/death. These processes contribute to formation of lineage-specific gene family expansions that commonly occupy subtelomeres across eukaryotes. Investigating the evolution of subtelomeric gene families is complicated by the presence of repetitive DNA and high sequence similarity among gene family members that prevents accurate assembly from whole genome sequences. Here, we investigated the evolution of the telomere-associated (TLO) gene family in Candida albicans using 189 complete coding sequences retrieved from 23 genetically diverse strains across the species. Tlo genes conformed to the 3 major architectural groups (α/β/γ) previously defined in the genome reference strain but significantly differed in the degree of within-group diversity. One group, Tloβ, was always found at the same chromosome arm with strong sequence similarity among all strains. In contrast, diverse Tloα sequences have proliferated among chromosome arms. Tloγ genes formed 7 primary clades that included each of the previously identified Tloγ genes from the genome reference strain with 3 Tloγ genes always found on the same chromosome arm among strains. Architectural groups displayed regions of high conservation that resolved newly identified functional motifs, providing insight into potential regulatory mechanisms that distinguish groups. Thus, by resolving intraspecies subtelomeric gene variation, it is possible to identify previously unknown gene family complexity that may underpin adaptive functional variation.
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spelling pubmed-97134012022-12-02 Architectural groups of a subtelomeric gene family evolve along distinct paths in Candida albicans Dunn, Matthew J Shazib, Shahed U A Simonton, Emily Slot, Jason C Anderson, Matthew Z G3 (Bethesda) Investigation Subtelomeres are dynamic genomic regions shaped by elevated rates of recombination, mutation, and gene birth/death. These processes contribute to formation of lineage-specific gene family expansions that commonly occupy subtelomeres across eukaryotes. Investigating the evolution of subtelomeric gene families is complicated by the presence of repetitive DNA and high sequence similarity among gene family members that prevents accurate assembly from whole genome sequences. Here, we investigated the evolution of the telomere-associated (TLO) gene family in Candida albicans using 189 complete coding sequences retrieved from 23 genetically diverse strains across the species. Tlo genes conformed to the 3 major architectural groups (α/β/γ) previously defined in the genome reference strain but significantly differed in the degree of within-group diversity. One group, Tloβ, was always found at the same chromosome arm with strong sequence similarity among all strains. In contrast, diverse Tloα sequences have proliferated among chromosome arms. Tloγ genes formed 7 primary clades that included each of the previously identified Tloγ genes from the genome reference strain with 3 Tloγ genes always found on the same chromosome arm among strains. Architectural groups displayed regions of high conservation that resolved newly identified functional motifs, providing insight into potential regulatory mechanisms that distinguish groups. Thus, by resolving intraspecies subtelomeric gene variation, it is possible to identify previously unknown gene family complexity that may underpin adaptive functional variation. Oxford University Press 2022-10-21 /pmc/articles/PMC9713401/ /pubmed/36269198 http://dx.doi.org/10.1093/g3journal/jkac283 Text en © The Author(s) 2022. Published by Oxford University Press on behalf of Genetics Society of America. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Investigation
Dunn, Matthew J
Shazib, Shahed U A
Simonton, Emily
Slot, Jason C
Anderson, Matthew Z
Architectural groups of a subtelomeric gene family evolve along distinct paths in Candida albicans
title Architectural groups of a subtelomeric gene family evolve along distinct paths in Candida albicans
title_full Architectural groups of a subtelomeric gene family evolve along distinct paths in Candida albicans
title_fullStr Architectural groups of a subtelomeric gene family evolve along distinct paths in Candida albicans
title_full_unstemmed Architectural groups of a subtelomeric gene family evolve along distinct paths in Candida albicans
title_short Architectural groups of a subtelomeric gene family evolve along distinct paths in Candida albicans
title_sort architectural groups of a subtelomeric gene family evolve along distinct paths in candida albicans
topic Investigation
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9713401/
https://www.ncbi.nlm.nih.gov/pubmed/36269198
http://dx.doi.org/10.1093/g3journal/jkac283
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