Show simple item record

dc.contributor.authorLange, Julian
dc.contributor.authorSkaletsky, Helen
dc.contributor.authorvan Daalen, Saskia K.M.
dc.contributor.authorEmbry, Stephanie L.
dc.contributor.authorKorver, Cindy M.
dc.contributor.authorBrown, Laura G.
dc.contributor.authorOates, Robert D.
dc.contributor.authorSilber, Sherman
dc.contributor.authorRepping, Sjoerd
dc.contributor.authorPage, David C
dc.date.accessioned2015-03-31T17:31:00Z
dc.date.available2015-03-31T17:31:00Z
dc.date.issued2009-09
dc.date.submitted2009-07
dc.identifier.issn00928674
dc.identifier.issn1097-4172
dc.identifier.urihttp://hdl.handle.net/1721.1/96285
dc.description.abstractMassive palindromes in the human Y chromosome harbor mirror-image gene pairs essential for spermatogenesis. During evolution, these gene pairs have been maintained by intrapalindrome, arm-to-arm recombination. The mechanism of intrapalindrome recombination and risk of harmful effects are unknown. We report 51 patients with isodicentric Y (idicY) chromosomes formed by homologous crossing over between opposing arms of palindromes on sister chromatids. These ectopic recombination events occur at nearly all Y-linked palindromes. Based on our findings, we propose that intrapalindrome sequence identity is maintained via noncrossover pathways of homologous recombination. DNA double-strand breaks that initiate these pathways can be alternatively resolved by crossing over between sister chromatids to form idicY chromosomes, with clinical consequences ranging from spermatogenic failure to sex reversal and Turner syndrome. Our observations imply that crossover and noncrossover pathways are active in nearly all Y-linked palindromes, exposing an Achilles' heel in the mechanism that preserves palindrome-borne genes.en_US
dc.description.sponsorshipNational Institutes of Health (U.S.)en_US
dc.description.sponsorshipHoward Hughes Medical Instituteen_US
dc.description.sponsorshipNetherlands Organization for Scientific Researchen_US
dc.description.sponsorshipUniversity of Amsterdam. Academic Medical Centeren_US
dc.description.sponsorshipBoehringer Ingelheim (Fellowship)en_US
dc.language.isoen_US
dc.publisherElsevieren_US
dc.relation.isversionofhttp://dx.doi.org/10.1016/j.cell.2009.07.042en_US
dc.rightsArticle is made available in accordance with the publisher's policy and may be subject to US copyright law. Please refer to the publisher's site for terms of use.en_US
dc.sourceElsevieren_US
dc.titleIsodicentric Y Chromosomes and Sex Disorders as Byproducts of Homologous Recombination that Maintains Palindromesen_US
dc.typeArticleen_US
dc.identifier.citationLange, Julian, Helen Skaletsky, Saskia K.M. van Daalen, Stephanie L. Embry, Cindy M. Korver, Laura G. Brown, Robert D. Oates, Sherman Silber, Sjoerd Repping, and David C. Page. “Isodicentric Y Chromosomes and Sex Disorders as Byproducts of Homologous Recombination That Maintains Palindromes.” Cell 138, no. 5 (September 2009): 855–869. © 2009 Elsevier Inc.en_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Biologyen_US
dc.contributor.departmentWhitehead Institute for Biomedical Researchen_US
dc.contributor.mitauthorPage, David C.en_US
dc.contributor.mitauthorLange, Julianen_US
dc.contributor.mitauthorSkaletsky, Helenen_US
dc.contributor.mitauthorBrown, Laura G.en_US
dc.relation.journalCellen_US
dc.eprint.versionFinal published versionen_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dspace.orderedauthorsLange, Julian; Skaletsky, Helen; van Daalen, Saskia K.M.; Embry, Stephanie L.; Korver, Cindy M.; Brown, Laura G.; Oates, Robert D.; Silber, Sherman; Repping, Sjoerd; Page, David C.en_US
dc.identifier.orcidhttps://orcid.org/0000-0001-9920-3411
mit.licensePUBLISHER_POLICYen_US
mit.metadata.statusComplete


Files in this item

Thumbnail

This item appears in the following Collection(s)

Show simple item record