Shimojima Yamamoto Keiko, Tamura Takeaki, Okamoto Nobuhiko, Nishi Eriko, Noguchi Atsuko, Takahashi Ikuko, Sawaishi Yukio, Shimizu Masaki, Kanno Hitoshi, Minakuchi Yohei, Toyoda Atsushi, Yamamoto Toshiyuki
Department of Transfusion Medicine and Cell Processing, Tokyo Women's Medical University, Tokyo, 162-8666, Japan.
Institute of Medical Genetics, Tokyo Women's Medical University, Tokyo, 162-8666, Japan.
J Hum Genet. 2023 Nov;68(11):751-757. doi: 10.1038/s10038-023-01181-x. Epub 2023 Jul 10.
The mechanism of chromosomal rearrangement associated with inverted-duplication-deletion (INV-DUP-DEL) pattern formation has been investigated by many researchers, and several possible mechanisms have been proposed. Currently, fold-back and subsequent dicentric chromosome formation has been established as non-recurrent INV-DUP-DEL pattern formation mechanisms. In the present study, we analyzed the breakpoint junctions of INV-DUP-DEL patterns in five patients using long-read whole-genome sequencing and detected 2.2-6.1 kb copy-neutral regions in all five patients. At the end of the INV-DUP-DEL, two patients exhibited chromosomal translocations, which are recognized as telomere capture, and one patient showed direct telomere healing. The remaining two patients had additional small-sized intrachromosomal segments at the end of the derivative chromosomes. These findings have not been previously reported but they may only be explained by the presence of telomere capture breakage. Further investigations are required to better understand the mechanisms underlying this finding.
许多研究人员对与倒位重复缺失(INV-DUP-DEL)模式形成相关的染色体重排机制进行了研究,并提出了几种可能的机制。目前,回折和随后的双着丝粒染色体形成已被确立为非复发性INV-DUP-DEL模式形成机制。在本研究中,我们使用长读长全基因组测序分析了5例患者中INV-DUP-DEL模式的断点连接,在所有5例患者中均检测到2.2-6.1 kb的拷贝中性区域。在INV-DUP-DEL的末端,2例患者出现了染色体易位,即端粒捕获,1例患者表现为直接端粒愈合。其余2例患者在衍生染色体末端有额外的小尺寸染色体内片段。这些发现以前未曾报道过,但它们可能只能通过端粒捕获断裂的存在来解释。需要进一步研究以更好地理解这一发现背后的机制。