| Literature DB >> 9482573 |
M Yamamoto1, M P Keller, T Yasuda, K Hayasaka, A Ohnishi, H Yoshikawa, T Yanagihara, T Mitsuma, P F Chance, G Sobue.
Abstract
The CMT1A-REP repeat is proposed to mediate unequal crossover leading to a 1.5 Mb duplication in chromosome 17p11.2-12 associated with Charcot-Marie-Tooth neuropathy type 1A (CMT1A). There is an apparent recombinational "hotspot" in the CMT1A-REP repeat since the majority of crossover breakpoints for CMT1A are located within a 1.7 kb interval. Further to characterize the crossover breakpoint region, we constructed PCR primers that specifically amplify the duplication breakpoint junctions in a series of Japanese and Caucasian CMT1A patients. We mapped the breakpoints in 89% of patients within a 700 bp interval of the CMT1A-REP repeat. This 700 bp region is 1.3 kb telomeric to a previously described mariner-like transposable element. Our observations further define the location of crossovers for CMT1A and provide additional evidence that this region is a recombinational "hotspot" within the CMT1A-REP repeat.Entities:
Mesh:
Year: 1998 PMID: 9482573 DOI: 10.1002/(SICI)1098-1004(1998)11:2<109::AID-HUMU2>3.0.CO;2-E
Source DB: PubMed Journal: Hum Mutat ISSN: 1059-7794 Impact factor: 4.878