长读测序检测独特的DUP-TRP/INV-DUP结构。

IF 1.7 4区 生物学 Q3 GENETICS & HEREDITY
Rina Shimomura, Keiko Shimojima Yamamoto, Mutsuki Nakano, Takahiro Tayama, Tatsuo Mori, Eriko Nishi, Ken Inoue, Satoru Nagata, Nobuhiko Okamoto, Toshiyuki Yamamoto
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引用次数: 0

摘要

重复-三重复/反向重复(DUP-TRP/INV-DUP)是导致基因组重复的机制之一。DUP-TRP/INV-DUP有一些特点;在基因组拷贝数分析中,出现了信号log2比的移动平均值,其中心最高,两侧台阶较低;染色体结构仅由两个连接点组成;在重复序列的末端有反向重复序列,在同一侧有重复序列,在相反方向有重复序列;DUP-TRP/INV-DUP结构的大小一般在1mb以内。在本研究中,我们分析了两例涉及PLP1和MECP2的DUP-TRP/INV-DUP患者。进行全基因组长读测序,确认所有断点连接。患者1表现出典型的DUP-TRP/INV-DUP模式,涉及PLP1,而患者2在MECP2区域表现出独特的DUP-TRP/INV-DUP模式,涉及Xq22.3远端46 mb区域的额外染色体断裂。基于这一发现,我们怀疑Xq22.3染色体断裂是最初的损伤。检测到的两个断裂端被认为是通过与反向重复结构相邻的Xq28区域结合形成三次复制结构来修复的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Unique DUP-TRP/INV-DUP Structure Detected by Long-Read Sequencing.

Duplication-triplication/inverted-duplication (DUP-TRP/INV-DUP) is one of the mechanisms that causes genomic triplications. There are some characteristics of the DUP-TRP/INV-DUP; the appearance of a moving average of signal log2 ratio in genomic copy number analysis consisting of the highest center with lower steps on both sides; the chromosomal structure is composed of only two junctions; there are inverted repeats at the ends of the triplications and duplications on the same side and those connected in the opposite direction; and the size of the DUP-TRP/INV-DUP structure is generally less than the 1-Mb range. In this study, we analyzed two patients with DUP-TRP/INV-DUP involving PLP1 and MECP2. Whole-genome long-read sequencing was performed, and all breakpoint junctions were confirmed. Patient 1 showed a typical DUP-TRP/INV-DUP pattern involving PLP1, whereas Patient 2 showed a unique DUP-TRP/INV-DUP pattern in the MECP2 region, which involved additional chromosomal breakages at a 46-Mb far remote region of Xq22.3. Based on this finding, we suspected that chromosomal breakage at Xq22.3 was the initial damage. The detected two break ends were considered to be repaired by binding to the Xq28 region adjacent to the inverted repeat structure to form a triplication structure.

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来源期刊
CiteScore
3.50
自引率
5.00%
发文量
432
审稿时长
2-4 weeks
期刊介绍: The American Journal of Medical Genetics - Part A (AJMG) gives you continuous coverage of all biological and medical aspects of genetic disorders and birth defects, as well as in-depth documentation of phenotype analysis within the current context of genotype/phenotype correlations. In addition to Part A , AJMG also publishes two other parts: Part B: Neuropsychiatric Genetics , covering experimental and clinical investigations of the genetic mechanisms underlying neurologic and psychiatric disorders. Part C: Seminars in Medical Genetics , guest-edited collections of thematic reviews of topical interest to the readership of AJMG .
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