Making heads or tails of shattered chromosomes

Isolation of lagging chromosomes in micronuclei causes catastrophic genome rearrangements The human genome is subject to continuous change as a result of spontaneous DNA mutation. Most of the genetic changes are harmless, but occasionally they can disturb normal cell functioning and lead to cancer o...

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Published inScience (American Association for the Advancement of Science) Vol. 348; no. 6240; pp. 1205 - 1206
Main Author Kloosterman, Wigard P.
Format Journal Article
LanguageEnglish
Published Washington The American Association for the Advancement of Science 12.06.2015
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Abstract Isolation of lagging chromosomes in micronuclei causes catastrophic genome rearrangements The human genome is subject to continuous change as a result of spontaneous DNA mutation. Most of the genetic changes are harmless, but occasionally they can disturb normal cell functioning and lead to cancer or congenital diseases. Much of the novel genetic variation that arises in human genomes affects only one or a few nucleotides. However, catastrophic changes of genome structure, termed chromothripsis, can produce a dramatic reorganization of DNA on one or even several chromosomes. A recent study by Zhang et al. ( 1 ) has now revealed a molecular mechanism that causes chromothripsis.
AbstractList Isolation of lagging chromosomes in micronuclei causes catastrophic genome rearrangements The human genome is subject to continuous change as a result of spontaneous DNA mutation. Most of the genetic changes are harmless, but occasionally they can disturb normal cell functioning and lead to cancer or congenital diseases. Much of the novel genetic variation that arises in human genomes affects only one or a few nucleotides. However, catastrophic changes of genome structure, termed chromothripsis, can produce a dramatic reorganization of DNA on one or even several chromosomes. A recent study by Zhang et al. ( 1 ) has now revealed a molecular mechanism that causes chromothripsis.
The human genome is subject to continuous change as a result of spontaneous DNA mutation. Most of the genetic changes are harmless, but occasionally they can disturb normal cell functioning and lead to cancer or congenital diseases. Much of the novel genetic variation that arises in human genomes affects only one or a few nucleotides. However, catastrophic changes of genome structure, termed chromothripsis, can produce a dramatic reorganization of DNA on one or even several chromosomes. A recent study by Zhang et al. (1) has now revealed a molecular mechanism that causes chromothripsis.
The human genome is subject to continuous change as a result of spontaneous DNA mutation. Most of the genetic changes are harmless, but occasionally they can disturb normal cell functioning and lead to cancer or congenital diseases. Much of the novel genetic variation that arises in human genomes affects only one or a few nucleotides. However, catastrophic changes of genome structure, termed chromothripsis, can produce a dramatic reorganization of DNA on one or even several chromosomes. A recent study by Zhang et al. has now revealed a molecular mechanism that causes chromothripsis.
Author Kloosterman, Wigard P.
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10.1038/nature10802
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Snippet Isolation of lagging chromosomes in micronuclei causes catastrophic genome rearrangements The human genome is subject to continuous change as a result of...
The human genome is subject to continuous change as a result of spontaneous DNA mutation. Most of the genetic changes are harmless, but occasionally they can...
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SubjectTerms Cancer
Chromosomes
congenital abnormalities
Deoxyribonucleic acid
DNA
Genetic diversity
genetic variation
Genetics
genome
Genomes
Genomics
humans
Molecular biology
Molecular structure
Mutation
Mutations
neoplasms
Nucleotides
Title Making heads or tails of shattered chromosomes
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