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LIBRIS Formathandbok  (Information om MARC21)
FältnamnIndikatorerMetadata
00002686naa a2200289 4500
001oai:DiVA.org:su-32011
003SwePub
008091202s2009 | |||||||||||000 ||eng|
024a https://urn.kb.se/resolve?urn=urn:nbn:se:su:diva-320112 URI
024a https://doi.org/10.1093/mutage/gen0722 DOI
040 a (SwePub)su
041 a engb eng
042 9 SwePub
072 7a ref2 swepub-contenttype
072 7a art2 swepub-publicationtype
100a Gottipati, Ponnari4 aut
2451 0a Transcription-associated recombination in eukaryotes :b link between transcription, replication and recombination.
264 c 2009-01-12
264 1b Oxford University Press (OUP),c 2009
338 a print2 rdacarrier
520 a Homologous recombination (HR) is an important DNA repair pathway and is essential for cellular survival. It plays a major role in repairing replication-associated lesions and is functionally connected to replication. Transcription is another cellular process, which has emerged to have a connection with HR. Transcription enhances HR, which is a ubiquitous phenomenon referred to as transcription-associated recombination (TAR). Recent evidence suggests that TAR plays a role in inducing genetic instability, for example in the THO mutants (Tho2, Hpr1, Mft1 and Thp2) in yeast or during the development of the immune system leading to genetic diversity in mammals. On the other hand, evidence also suggests that TAR may play a role in preventing genetic instability in many different ways, one of which is by rescuing replication during transcription. Hence, TAR is a double-edged sword and plays a role in both preventing and inducing genetic instability. In spite of the interesting nature of TAR, the mechanism behind TAR has remained elusive. Recent advances in the area, however, suggest a link between TAR and replication and show specific genetic requirements for TAR that differ from regular HR. In this review, we aim to present the available evidence for TAR in both lower and higher eukaryotes and discuss its possible mechanisms, with emphasis on its connection with replication.
700a Helleday, Thomasu Stockholms universitet,Institutionen för genetik, mikrobiologi och toxikologi4 aut0 (Swepub:su)helleday
710a Stockholms universitetb Institutionen för genetik, mikrobiologi och toxikologi4 org
773t Mutagenesisd : Oxford University Press (OUP)g 24:3, s. 203-10q 24:3<203-10x 1464-3804x 0267-8357
856u https://academic.oup.com/mutage/article-pdf/24/3/203/3713562/gen072.pdf
8564 8u https://urn.kb.se/resolve?urn=urn:nbn:se:su:diva-32011
8564 8u https://doi.org/10.1093/mutage/gen072

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