Polymorphisms within the Telomerase Reverse Transcriptase gene (TERT) in four breeds of dogs selected for difference in lifespan and cancer susceptibility

Abstract Background Enzymatic activity of Te lomerase R everse T ranscriptase (TERT) is important in maintaining the telomere length and has been implicated in cancer and aging related pathology. Since cancer susceptibility as well as longevity of dogs vary between breeds, this study involved sequen...

Full description

Bibliographic Details
Main Authors: McAloney, Camille A, Silverstein, Kevin A T, Modiano, Jaime F, Bagchi, Anindya
Format: Article in Journal/Newspaper
Language:English
Published: BioMed Central Ltd. 2014
Subjects:
Online Access:http://www.biomedcentral.com/1746-6148/10/20
id ftbiomed:oai:biomedcentral.com:1746-6148-10-20
record_format openpolar
spelling ftbiomed:oai:biomedcentral.com:1746-6148-10-20 2023-05-15T17:22:30+02:00 Polymorphisms within the Telomerase Reverse Transcriptase gene (TERT) in four breeds of dogs selected for difference in lifespan and cancer susceptibility McAloney, Camille A Silverstein, Kevin A T Modiano, Jaime F Bagchi, Anindya 2014-01-14 http://www.biomedcentral.com/1746-6148/10/20 en eng BioMed Central Ltd. http://www.biomedcentral.com/1746-6148/10/20 Copyright 2014 McAloney et al.; licensee BioMed Central Ltd. Research article 2014 ftbiomed 2014-02-02T01:26:56Z Abstract Background Enzymatic activity of Te lomerase R everse T ranscriptase (TERT) is important in maintaining the telomere length and has been implicated in cancer and aging related pathology. Since cancer susceptibility as well as longevity of dogs vary between breeds, this study involved sequencing the entire TERT gene of Canis familiaris from DNA samples obtained from forty dogs, with ten dogs each of four breeds: Shih Tzu, Dachshund, Irish Wolfhound, and Newfoundland, each with different life expectancies and susceptibility to cancer. Results We compared the sequences of all forty individuals amongst one another and with the published sequence of canine TERT , and analyzed relationships between members of the same or different breeds. Two separate phylogenetic trees were generated and analyzed from these individuals. Polymorphisms were found most frequently in intronic regions of the gene, although exonic polymorphisms also were observed. In many locations genotypes were observed that were either homozygous for the reference sequence or heterozygous, but the variant homozygous genotype was not observed. Conclusions We propose that these homozygous variants are likely to have adverse effects in dogs. It was also found that the polymorphisms did not segregate by breed. Because the four breeds chosen come from geographically and physiologically distinct backgrounds, it can be inferred that the polymorphic diversification of TERT preceded breed derivation. Article in Journal/Newspaper Newfoundland BioMed Central
institution Open Polar
collection BioMed Central
op_collection_id ftbiomed
language English
description Abstract Background Enzymatic activity of Te lomerase R everse T ranscriptase (TERT) is important in maintaining the telomere length and has been implicated in cancer and aging related pathology. Since cancer susceptibility as well as longevity of dogs vary between breeds, this study involved sequencing the entire TERT gene of Canis familiaris from DNA samples obtained from forty dogs, with ten dogs each of four breeds: Shih Tzu, Dachshund, Irish Wolfhound, and Newfoundland, each with different life expectancies and susceptibility to cancer. Results We compared the sequences of all forty individuals amongst one another and with the published sequence of canine TERT , and analyzed relationships between members of the same or different breeds. Two separate phylogenetic trees were generated and analyzed from these individuals. Polymorphisms were found most frequently in intronic regions of the gene, although exonic polymorphisms also were observed. In many locations genotypes were observed that were either homozygous for the reference sequence or heterozygous, but the variant homozygous genotype was not observed. Conclusions We propose that these homozygous variants are likely to have adverse effects in dogs. It was also found that the polymorphisms did not segregate by breed. Because the four breeds chosen come from geographically and physiologically distinct backgrounds, it can be inferred that the polymorphic diversification of TERT preceded breed derivation.
format Article in Journal/Newspaper
author McAloney, Camille A
Silverstein, Kevin A T
Modiano, Jaime F
Bagchi, Anindya
spellingShingle McAloney, Camille A
Silverstein, Kevin A T
Modiano, Jaime F
Bagchi, Anindya
Polymorphisms within the Telomerase Reverse Transcriptase gene (TERT) in four breeds of dogs selected for difference in lifespan and cancer susceptibility
author_facet McAloney, Camille A
Silverstein, Kevin A T
Modiano, Jaime F
Bagchi, Anindya
author_sort McAloney, Camille A
title Polymorphisms within the Telomerase Reverse Transcriptase gene (TERT) in four breeds of dogs selected for difference in lifespan and cancer susceptibility
title_short Polymorphisms within the Telomerase Reverse Transcriptase gene (TERT) in four breeds of dogs selected for difference in lifespan and cancer susceptibility
title_full Polymorphisms within the Telomerase Reverse Transcriptase gene (TERT) in four breeds of dogs selected for difference in lifespan and cancer susceptibility
title_fullStr Polymorphisms within the Telomerase Reverse Transcriptase gene (TERT) in four breeds of dogs selected for difference in lifespan and cancer susceptibility
title_full_unstemmed Polymorphisms within the Telomerase Reverse Transcriptase gene (TERT) in four breeds of dogs selected for difference in lifespan and cancer susceptibility
title_sort polymorphisms within the telomerase reverse transcriptase gene (tert) in four breeds of dogs selected for difference in lifespan and cancer susceptibility
publisher BioMed Central Ltd.
publishDate 2014
url http://www.biomedcentral.com/1746-6148/10/20
genre Newfoundland
genre_facet Newfoundland
op_relation http://www.biomedcentral.com/1746-6148/10/20
op_rights Copyright 2014 McAloney et al.; licensee BioMed Central Ltd.
_version_ 1766109210017267712