Genomic restructuring in the Tasmanian devil facial tumour: chromosome painting and gene mapping provide clues to evolution of a transmissible tumour.

Devil facial tumour disease (DFTD) is a fatal, transmissible malignancy that threatens the world's largest marsupial carnivore, the Tasmanian devil, with extinction. First recognised in 1996, DFTD has had a catastrophic effect on wild devil numbers, and intense research efforts to understand an...

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Main Authors: Janine E Deakin, Hannah S Bender, Anne-Maree Pearse, Willem Rens, Patricia C M O'Brien, Malcolm A Ferguson-Smith, Yuanyuan Cheng, Katrina Morris, Robyn Taylor, Andrew Stuart, Katherine Belov, Chris T Amemiya, Elizabeth P Murchison, Anthony T Papenfuss, Jennifer A Marshall Graves
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2012-01-01
Series:PLoS Genetics
Online Access:http://europepmc.org/articles/PMC3280961?pdf=render
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spelling doaj-f4d44e8a61f54742aee37a9f9e9043d22020-11-25T02:36:32ZengPublic Library of Science (PLoS)PLoS Genetics1553-73901553-74042012-01-0182e100248310.1371/journal.pgen.1002483Genomic restructuring in the Tasmanian devil facial tumour: chromosome painting and gene mapping provide clues to evolution of a transmissible tumour.Janine E DeakinHannah S BenderAnne-Maree PearseWillem RensPatricia C M O'BrienMalcolm A Ferguson-SmithYuanyuan ChengKatrina MorrisRobyn TaylorAndrew StuartKatherine BelovChris T AmemiyaElizabeth P MurchisonAnthony T PapenfussJennifer A Marshall GravesDevil facial tumour disease (DFTD) is a fatal, transmissible malignancy that threatens the world's largest marsupial carnivore, the Tasmanian devil, with extinction. First recognised in 1996, DFTD has had a catastrophic effect on wild devil numbers, and intense research efforts to understand and contain the disease have since demonstrated that the tumour is a clonal cell line transmitted by allograft. We used chromosome painting and gene mapping to deconstruct the DFTD karyotype and determine the chromosome and gene rearrangements involved in carcinogenesis. Chromosome painting on three different DFTD tumour strains determined the origins of marker chromosomes and provided a general overview of the rearrangement in DFTD karyotypes. Mapping of 105 BAC clones by fluorescence in situ hybridisation provided a finer level of resolution of genome rearrangements in DFTD strains. Our findings demonstrate that only limited regions of the genome, mainly chromosomes 1 and X, are rearranged in DFTD. Regions rearranged in DFTD are also highly rearranged between different marsupials. Differences between strains are limited, reflecting the unusually stable nature of DFTD. Finally, our detailed maps of both the devil and tumour karyotypes provide a physical framework for future genomic investigations into DFTD.http://europepmc.org/articles/PMC3280961?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Janine E Deakin
Hannah S Bender
Anne-Maree Pearse
Willem Rens
Patricia C M O'Brien
Malcolm A Ferguson-Smith
Yuanyuan Cheng
Katrina Morris
Robyn Taylor
Andrew Stuart
Katherine Belov
Chris T Amemiya
Elizabeth P Murchison
Anthony T Papenfuss
Jennifer A Marshall Graves
spellingShingle Janine E Deakin
Hannah S Bender
Anne-Maree Pearse
Willem Rens
Patricia C M O'Brien
Malcolm A Ferguson-Smith
Yuanyuan Cheng
Katrina Morris
Robyn Taylor
Andrew Stuart
Katherine Belov
Chris T Amemiya
Elizabeth P Murchison
Anthony T Papenfuss
Jennifer A Marshall Graves
Genomic restructuring in the Tasmanian devil facial tumour: chromosome painting and gene mapping provide clues to evolution of a transmissible tumour.
PLoS Genetics
author_facet Janine E Deakin
Hannah S Bender
Anne-Maree Pearse
Willem Rens
Patricia C M O'Brien
Malcolm A Ferguson-Smith
Yuanyuan Cheng
Katrina Morris
Robyn Taylor
Andrew Stuart
Katherine Belov
Chris T Amemiya
Elizabeth P Murchison
Anthony T Papenfuss
Jennifer A Marshall Graves
author_sort Janine E Deakin
title Genomic restructuring in the Tasmanian devil facial tumour: chromosome painting and gene mapping provide clues to evolution of a transmissible tumour.
title_short Genomic restructuring in the Tasmanian devil facial tumour: chromosome painting and gene mapping provide clues to evolution of a transmissible tumour.
title_full Genomic restructuring in the Tasmanian devil facial tumour: chromosome painting and gene mapping provide clues to evolution of a transmissible tumour.
title_fullStr Genomic restructuring in the Tasmanian devil facial tumour: chromosome painting and gene mapping provide clues to evolution of a transmissible tumour.
title_full_unstemmed Genomic restructuring in the Tasmanian devil facial tumour: chromosome painting and gene mapping provide clues to evolution of a transmissible tumour.
title_sort genomic restructuring in the tasmanian devil facial tumour: chromosome painting and gene mapping provide clues to evolution of a transmissible tumour.
publisher Public Library of Science (PLoS)
series PLoS Genetics
issn 1553-7390
1553-7404
publishDate 2012-01-01
description Devil facial tumour disease (DFTD) is a fatal, transmissible malignancy that threatens the world's largest marsupial carnivore, the Tasmanian devil, with extinction. First recognised in 1996, DFTD has had a catastrophic effect on wild devil numbers, and intense research efforts to understand and contain the disease have since demonstrated that the tumour is a clonal cell line transmitted by allograft. We used chromosome painting and gene mapping to deconstruct the DFTD karyotype and determine the chromosome and gene rearrangements involved in carcinogenesis. Chromosome painting on three different DFTD tumour strains determined the origins of marker chromosomes and provided a general overview of the rearrangement in DFTD karyotypes. Mapping of 105 BAC clones by fluorescence in situ hybridisation provided a finer level of resolution of genome rearrangements in DFTD strains. Our findings demonstrate that only limited regions of the genome, mainly chromosomes 1 and X, are rearranged in DFTD. Regions rearranged in DFTD are also highly rearranged between different marsupials. Differences between strains are limited, reflecting the unusually stable nature of DFTD. Finally, our detailed maps of both the devil and tumour karyotypes provide a physical framework for future genomic investigations into DFTD.
url http://europepmc.org/articles/PMC3280961?pdf=render
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