Transcriptome sequencing reveals signatures of positive selection in the Spot-Tailed Earless Lizard.

The continual loss of threatened biodiversity is occurring at an accelerated pace. High-throughput sequencing technologies are now providing opportunities to address this issue by aiding in the generation of molecular data for many understudied species of high conservation interest. Our overall goal...

Full description

Bibliographic Details
Main Authors: Jose A Maldonado, Thomas J Firneno, Corey E Roelke, Nathan D Rains, Juliet Mwgiri, Matthew K Fujita
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2020-01-01
Series:PLoS ONE
Online Access:https://doi.org/10.1371/journal.pone.0234504
_version_ 1819199561107767296
author Jose A Maldonado
Thomas J Firneno
Corey E Roelke
Nathan D Rains
Juliet Mwgiri
Matthew K Fujita
author_facet Jose A Maldonado
Thomas J Firneno
Corey E Roelke
Nathan D Rains
Juliet Mwgiri
Matthew K Fujita
author_sort Jose A Maldonado
collection DOAJ
description The continual loss of threatened biodiversity is occurring at an accelerated pace. High-throughput sequencing technologies are now providing opportunities to address this issue by aiding in the generation of molecular data for many understudied species of high conservation interest. Our overall goal of this study was to begin building the genomic resources to continue investigations and conservation of the Spot-Tailed Earless lizard. Here we leverage the power of high-throughput sequencing to generate the liver transcriptome for the Northern Spot-Tailed Earless Lizard (Holbrookia lacerata) and Southern Spot-Tailed Earless Lizard (Holbrookia subcaudalis), which have declined in abundance in the past decades, and their sister species, the Common Lesser Earless Lizard (Holbrookia maculata). Our efforts produced high quality and robust transcriptome assemblies validated by 1) quantifying the number of processed reads represented in the transcriptome assembly and 2) quantifying the number of highly conserved single-copy orthologs that are present in our transcript set using the BUSCO pipeline. We found 1,361 1-to-1 orthologs among the three Holbrookia species, Anolis carolinensis, and Sceloporus undulatus. We carried out dN/dS selection tests using a branch-sites model and identified a dozen genes that experienced positive selection in the Holbrookia lineage with functions in development, immunity, and metabolism. Our single-copy orthologous sequences additionally revealed significant pairwise sequence divergence (~.73%) between the Northern H. lacerata and Southern H. subcaudalis that further supports the recent elevation of the Southern Spot-Tailed Earless Lizard to full species.
first_indexed 2024-12-23T03:18:17Z
format Article
id doaj.art-f67750780a444d4885d0fc80338b2b37
institution Directory Open Access Journal
issn 1932-6203
language English
last_indexed 2024-12-23T03:18:17Z
publishDate 2020-01-01
publisher Public Library of Science (PLoS)
record_format Article
series PLoS ONE
spelling doaj.art-f67750780a444d4885d0fc80338b2b372022-12-21T18:02:03ZengPublic Library of Science (PLoS)PLoS ONE1932-62032020-01-01156e023450410.1371/journal.pone.0234504Transcriptome sequencing reveals signatures of positive selection in the Spot-Tailed Earless Lizard.Jose A MaldonadoThomas J FirnenoCorey E RoelkeNathan D RainsJuliet MwgiriMatthew K FujitaThe continual loss of threatened biodiversity is occurring at an accelerated pace. High-throughput sequencing technologies are now providing opportunities to address this issue by aiding in the generation of molecular data for many understudied species of high conservation interest. Our overall goal of this study was to begin building the genomic resources to continue investigations and conservation of the Spot-Tailed Earless lizard. Here we leverage the power of high-throughput sequencing to generate the liver transcriptome for the Northern Spot-Tailed Earless Lizard (Holbrookia lacerata) and Southern Spot-Tailed Earless Lizard (Holbrookia subcaudalis), which have declined in abundance in the past decades, and their sister species, the Common Lesser Earless Lizard (Holbrookia maculata). Our efforts produced high quality and robust transcriptome assemblies validated by 1) quantifying the number of processed reads represented in the transcriptome assembly and 2) quantifying the number of highly conserved single-copy orthologs that are present in our transcript set using the BUSCO pipeline. We found 1,361 1-to-1 orthologs among the three Holbrookia species, Anolis carolinensis, and Sceloporus undulatus. We carried out dN/dS selection tests using a branch-sites model and identified a dozen genes that experienced positive selection in the Holbrookia lineage with functions in development, immunity, and metabolism. Our single-copy orthologous sequences additionally revealed significant pairwise sequence divergence (~.73%) between the Northern H. lacerata and Southern H. subcaudalis that further supports the recent elevation of the Southern Spot-Tailed Earless Lizard to full species.https://doi.org/10.1371/journal.pone.0234504
spellingShingle Jose A Maldonado
Thomas J Firneno
Corey E Roelke
Nathan D Rains
Juliet Mwgiri
Matthew K Fujita
Transcriptome sequencing reveals signatures of positive selection in the Spot-Tailed Earless Lizard.
PLoS ONE
title Transcriptome sequencing reveals signatures of positive selection in the Spot-Tailed Earless Lizard.
title_full Transcriptome sequencing reveals signatures of positive selection in the Spot-Tailed Earless Lizard.
title_fullStr Transcriptome sequencing reveals signatures of positive selection in the Spot-Tailed Earless Lizard.
title_full_unstemmed Transcriptome sequencing reveals signatures of positive selection in the Spot-Tailed Earless Lizard.
title_short Transcriptome sequencing reveals signatures of positive selection in the Spot-Tailed Earless Lizard.
title_sort transcriptome sequencing reveals signatures of positive selection in the spot tailed earless lizard
url https://doi.org/10.1371/journal.pone.0234504
work_keys_str_mv AT joseamaldonado transcriptomesequencingrevealssignaturesofpositiveselectioninthespottailedearlesslizard
AT thomasjfirneno transcriptomesequencingrevealssignaturesofpositiveselectioninthespottailedearlesslizard
AT coreyeroelke transcriptomesequencingrevealssignaturesofpositiveselectioninthespottailedearlesslizard
AT nathandrains transcriptomesequencingrevealssignaturesofpositiveselectioninthespottailedearlesslizard
AT julietmwgiri transcriptomesequencingrevealssignaturesofpositiveselectioninthespottailedearlesslizard
AT matthewkfujita transcriptomesequencingrevealssignaturesofpositiveselectioninthespottailedearlesslizard