Large-scale variation in single nucleotide polymorphism density within the laboratory axolotl (Ambystoma mexicanum).


Journal

Developmental dynamics : an official publication of the American Association of Anatomists
ISSN: 1097-0177
Titre abrégé: Dev Dyn
Pays: United States
ID NLM: 9201927

Informations de publication

Date de publication:
06 2021
Historique:
revised: 14 09 2020
received: 01 07 2020
accepted: 24 09 2020
pubmed: 2 10 2020
medline: 11 3 2022
entrez: 1 10 2020
Statut: ppublish

Résumé

Recent efforts to assemble and analyze the Ambystoma mexicanum genome have dramatically improved the potential to develop molecular tools and pursue genome-wide analyses of genetic variation. To better resolve the distribution and origins of genetic variation with A mexicanum, we compared DNA sequence data for two laboratory A mexicanum and one A tigrinum to identify 702 million high confidence polymorphisms distributed across the 32 Gb genome. While the wild-caught A tigrinum was generally more polymorphic in a genome-wide sense, several multi-megabase regions were identified from A mexicanum genomes that were actually more polymorphic than A tigrinum. Analysis of polymorphism and repeat content reveals that these regions likely originated from the intentional hybridization of A mexicanum and A tigrinum that was used to introduce the albino mutation into laboratory stocks. Our findings show that axolotl genomes are variable with respect to introgressed DNA from a highly polymorphic species. It seems likely that other divergent regions will be discovered with additional sequencing of A mexicanum. This has practical implications for designing molecular probes and suggests a need to study A mexicanum phenotypic variation and genome evolution across the tiger salamander clade.

Sections du résumé

BACKGROUND
Recent efforts to assemble and analyze the Ambystoma mexicanum genome have dramatically improved the potential to develop molecular tools and pursue genome-wide analyses of genetic variation.
RESULTS
To better resolve the distribution and origins of genetic variation with A mexicanum, we compared DNA sequence data for two laboratory A mexicanum and one A tigrinum to identify 702 million high confidence polymorphisms distributed across the 32 Gb genome. While the wild-caught A tigrinum was generally more polymorphic in a genome-wide sense, several multi-megabase regions were identified from A mexicanum genomes that were actually more polymorphic than A tigrinum. Analysis of polymorphism and repeat content reveals that these regions likely originated from the intentional hybridization of A mexicanum and A tigrinum that was used to introduce the albino mutation into laboratory stocks.
CONCLUSIONS
Our findings show that axolotl genomes are variable with respect to introgressed DNA from a highly polymorphic species. It seems likely that other divergent regions will be discovered with additional sequencing of A mexicanum. This has practical implications for designing molecular probes and suggests a need to study A mexicanum phenotypic variation and genome evolution across the tiger salamander clade.

Identifiants

pubmed: 33001517
doi: 10.1002/dvdy.257
pmc: PMC8715502
mid: NIHMS1764885
doi:

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, U.S. Gov't, Non-P.H.S.

Langues

eng

Sous-ensembles de citation

IM

Pagination

822-837

Subventions

Organisme : NIH HHS
ID : P40 OD019794
Pays : United States
Organisme : NIH HHS
ID : R24 OD010435
Pays : United States
Organisme : NIGMS NIH HHS
ID : R35 GM130349
Pays : United States

Informations de copyright

© 2020 Wiley Periodicals LLC.

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Auteurs

Nataliya Timoshevskaya (N)

Department of Biology, University of Kentucky, Lexington, Kentucky, USA.

S Randal Voss (SR)

Spinal Cord and Brain Injury Research Center, University of Kentucky, Lexington, Kentucky, USA.
Department of Neuroscience, University of Kentucky, Lexington, Kentucky, USA.
Ambystoma Genetic Stock Center, University of Kentucky, Lexington, Kentucky, USA.

Caitlin N Labianca (CN)

Paul Laurence Dunbar High School, Lexington, Kentucky, USA.
Current Affiliation: Department of Biology, University of Rochester, Rochester, New York, USA.

Cassity R High (CR)

Spinal Cord and Brain Injury Research Center, University of Kentucky, Lexington, Kentucky, USA.
Department of Neuroscience, University of Kentucky, Lexington, Kentucky, USA.

Jeramiah J Smith (JJ)

Department of Biology, University of Kentucky, Lexington, Kentucky, USA.

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