Beck Christine R, Carvalho Claudia M B, Banser Linda, Gambin Tomasz, Stubbolo Danielle, Yuan Bo, Sperle Karen, McCahan Suzanne M, Henneke Marco, Seeman Pavel, Garbern James Y, Hobson Grace M, Lupski James R
Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, United States of America.
Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, United States of America; Centro de Pesquisas Rene Rachou- FIOCRUZ, Belo Horizonte, Minas Gerais, Brazil.
PLoS Genet. 2015 Mar 6;11(3):e1005050. doi: 10.1371/journal.pgen.1005050. eCollection 2015 Mar.
Inverted repeats (IRs) can facilitate structural variation as crucibles of genomic rearrangement. Complex duplication-inverted triplication-duplication (DUP-TRP/INV-DUP) rearrangements that contain breakpoint junctions within IRs have been recently associated with both MECP2 duplication syndrome (MIM#300260) and Pelizaeus-Merzbacher disease (PMD, MIM#312080). We investigated 17 unrelated PMD subjects with copy number gains at the PLP1 locus including triplication and quadruplication of specific genomic intervals-16/17 were found to have a DUP-TRP/INV-DUP rearrangement product. An IR distal to PLP1 facilitates DUP-TRP/INV-DUP formation as well as an inversion structural variation found frequently amongst normal individuals. We show that a homology-or homeology-driven replicative mechanism of DNA repair can apparently mediate template switches within stretches of microhomology. Moreover, we provide evidence that quadruplication and potentially higher order amplification of a genomic interval can occur in a manner consistent with rolling circle amplification as predicted by the microhomology-mediated break induced replication (MMBIR) model.
反向重复序列(IRs)作为基因组重排的熔炉,可促进结构变异。最近发现,在IRs内含有断点连接的复杂重复-反向三倍体-重复(DUP-TRP/INV-DUP)重排与MECP2重复综合征(MIM#300260)和佩利措伊斯-梅茨巴赫病(PMD,MIM#312080)均有关联。我们对17名在PLP1基因座存在拷贝数增加(包括特定基因组区间的三倍体和四倍体)的无血缘关系的PMD患者进行了研究,结果发现其中16/17例具有DUP-TRP/INV-DUP重排产物。PLP1远端的一个IR促进了DUP-TRP/INV-DUP的形成以及在正常个体中频繁发现的一种倒位结构变异。我们表明,一种由同源性或准同源性驱动的DNA修复复制机制显然可以介导微同源性片段内的模板转换。此外,我们提供的证据表明,基因组区间的四倍体化以及可能的更高阶扩增能够以与微同源性介导的断裂诱导复制(MMBIR)模型所预测的滚环扩增一致的方式发生。