dc.contributor.author | Lange, Julian | |
dc.contributor.author | Skaletsky, Helen | |
dc.contributor.author | van Daalen, Saskia K.M. | |
dc.contributor.author | Embry, Stephanie L. | |
dc.contributor.author | Korver, Cindy M. | |
dc.contributor.author | Brown, Laura G. | |
dc.contributor.author | Oates, Robert D. | |
dc.contributor.author | Silber, Sherman | |
dc.contributor.author | Repping, Sjoerd | |
dc.contributor.author | Page, David C | |
dc.date.accessioned | 2015-03-31T17:31:00Z | |
dc.date.available | 2015-03-31T17:31:00Z | |
dc.date.issued | 2009-09 | |
dc.date.submitted | 2009-07 | |
dc.identifier.issn | 00928674 | |
dc.identifier.issn | 1097-4172 | |
dc.identifier.uri | http://hdl.handle.net/1721.1/96285 | |
dc.description.abstract | Massive 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.sponsorship | National Institutes of Health (U.S.) | en_US |
dc.description.sponsorship | Howard Hughes Medical Institute | en_US |
dc.description.sponsorship | Netherlands Organization for Scientific Research | en_US |
dc.description.sponsorship | University of Amsterdam. Academic Medical Center | en_US |
dc.description.sponsorship | Boehringer Ingelheim (Fellowship) | en_US |
dc.language.iso | en_US | |
dc.publisher | Elsevier | en_US |
dc.relation.isversionof | http://dx.doi.org/10.1016/j.cell.2009.07.042 | en_US |
dc.rights | Article 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.source | Elsevier | en_US |
dc.title | Isodicentric Y Chromosomes and Sex Disorders as Byproducts of Homologous Recombination that Maintains Palindromes | en_US |
dc.type | Article | en_US |
dc.identifier.citation | Lange, 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.department | Massachusetts Institute of Technology. Department of Biology | en_US |
dc.contributor.department | Whitehead Institute for Biomedical Research | en_US |
dc.contributor.mitauthor | Page, David C. | en_US |
dc.contributor.mitauthor | Lange, Julian | en_US |
dc.contributor.mitauthor | Skaletsky, Helen | en_US |
dc.contributor.mitauthor | Brown, Laura G. | en_US |
dc.relation.journal | Cell | en_US |
dc.eprint.version | Final published version | en_US |
dc.type.uri | http://purl.org/eprint/type/JournalArticle | en_US |
eprint.status | http://purl.org/eprint/status/PeerReviewed | en_US |
dspace.orderedauthors | Lange, 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.orcid | https://orcid.org/0000-0001-9920-3411 | |
mit.license | PUBLISHER_POLICY | en_US |
mit.metadata.status | Complete | |