Literature DB >> 32488466

The involvement of U-type dicentric chromosomes in the formation of terminal deletions with or without adjacent inverted duplications.

Takema Kato1, Hidehito Inagaki1, Syunsuke Miyai1, Fumihiko Suzuki1, Yuki Naru1, Yasuko Shinkai1, Asuka Kato1, Kazuo Kanyama1, Seiji Mizuno2, Yukako Muramatsu3, Toshiyuki Yamamoto4, Mitsuhisa Shinya5,6, Yukiko Tazaki5,6, Sayuri Hiwatashi5,6, Toshiro Ikeda5,6, Mamoru Ozaki7, Hiroki Kurahashi8,9.   

Abstract

An inverted duplication with a terminal deletion (inv-dup-del) is one of the complex constitutional structural rearrangements that can occur in a chromosome. Although breakages of dicentric chromosome have been suggested, the precise mechanism of this is yet to be fully understood. In our present study, we investigated the genomic structure of 10 inv-dup-del cases to elucidate this mechanism. Two recurrent 8p inv-dup-del cases harbored a large copy-number-neutral region between the duplication and deletion in common. Although the other non-recurrent cases did not appear to have this copy-number-neutral region, refined sequencing analysis identified that they contained a small intervening region at the junction between the inverted and non-inverted segment. The size of this small intervening region ranged from 1741 to 3728 bp. Combined with a presence of microhomology at the junction, a resolution of the replication fork stalling through template switching within the same replication fork is suggested. We further observed two cases with mosaicism of the dicentric chromosome and various structural rearrangements related to the dicentric chromosome. Refined analysis allowed us to identify different breakpoints on the same chromosome in the same case, implicating multiple rounds of U-type formation and its breakage. From these results, we propose that a replication-based mechanism generates unstable dicentric chromosomes and that their breakage leads to the formation of inv-dup-dels and other related derivative chromosomes.

Entities:  

Year:  2020        PMID: 32488466     DOI: 10.1007/s00439-020-02186-8

Source DB:  PubMed          Journal:  Hum Genet        ISSN: 0340-6717            Impact factor:   4.132


  5 in total

Review 1.  Mechanisms of structural chromosomal rearrangement formation.

Authors:  Bruna Burssed; Malú Zamariolli; Fernanda Teixeira Bellucco; Maria Isabel Melaragno
Journal:  Mol Cytogenet       Date:  2022-06-14       Impact factor: 1.904

2.  8p23.2-pter Microdeletions: Seven New Cases Narrowing the Candidate Region and Review of the Literature.

Authors:  Ilaria Catusi; Maria Garzo; Anna Paola Capra; Silvana Briuglia; Chiara Baldo; Maria Paola Canevini; Rachele Cantone; Flaviana Elia; Francesca Forzano; Ornella Galesi; Enrico Grosso; Michela Malacarne; Angela Peron; Corrado Romano; Monica Saccani; Lidia Larizza; Maria Paola Recalcati
Journal:  Genes (Basel)       Date:  2021-04-27       Impact factor: 4.096

3.  Clinical significance and mechanisms associated with segmental UPD.

Authors:  Peter R Papenhausen; Carla A Kelly; Samuel Harris; Samantha Caldwell; Stuart Schwartz; Andrea Penton
Journal:  Mol Cytogenet       Date:  2021-07-20       Impact factor: 2.009

4.  Clinical Manifestations of Various Molecular Cytogenetic Variants of Eight Cases of "8p Inverted Duplication/Deletion Syndrome".

Authors:  Darya A Yurchenko; Marina E Minzhenkova; Elena L Dadali; Zhanna G Markova; Galina E Rudenskaya; Galina N Matyushchenko; Ilya V Kanivets; Nadezda V Shilova
Journal:  Biomedicines       Date:  2022-02-28

5.  Characterization of Chromosomal Breakpoints in 12 Cases with 8p Rearrangements Defines a Continuum of Fragility of the Region.

Authors:  Serena Redaelli; Donatella Conconi; Elena Sala; Nicoletta Villa; Francesca Crosti; Gaia Roversi; Ilaria Catusi; Chiara Valtorta; Maria Paola Recalcati; Leda Dalprà; Marialuisa Lavitrano; Angela Bentivegna
Journal:  Int J Mol Sci       Date:  2022-03-20       Impact factor: 5.923

  5 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.