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The involvement of U-type dicentric chromosomes in the formation of terminal deletions with or without adjacent inverted duplications.
Kato, Takema; Inagaki, Hidehito; Miyai, Syunsuke; Suzuki, Fumihiko; Naru, Yuki; Shinkai, Yasuko; Kato, Asuka; Kanyama, Kazuo; Mizuno, Seiji; Muramatsu, Yukako; Yamamoto, Toshiyuki; Shinya, Mitsuhisa; Tazaki, Yukiko; Hiwatashi, Sayuri; Ikeda, Toshiro; Ozaki, Mamoru; Kurahashi, Hiroki.
Afiliación
  • Kato T; Division of Molecular Genetics, Institute for Comprehensive Medical Science, Fujita Health University, 1-98 Dengakugakubo, Kutsukake-cho, Toyoake, Aichi, 470-1192, Japan.
  • Inagaki H; Division of Molecular Genetics, Institute for Comprehensive Medical Science, Fujita Health University, 1-98 Dengakugakubo, Kutsukake-cho, Toyoake, Aichi, 470-1192, Japan.
  • Miyai S; Division of Molecular Genetics, Institute for Comprehensive Medical Science, Fujita Health University, 1-98 Dengakugakubo, Kutsukake-cho, Toyoake, Aichi, 470-1192, Japan.
  • Suzuki F; Division of Molecular Genetics, Institute for Comprehensive Medical Science, Fujita Health University, 1-98 Dengakugakubo, Kutsukake-cho, Toyoake, Aichi, 470-1192, Japan.
  • Naru Y; Division of Molecular Genetics, Institute for Comprehensive Medical Science, Fujita Health University, 1-98 Dengakugakubo, Kutsukake-cho, Toyoake, Aichi, 470-1192, Japan.
  • Shinkai Y; Division of Molecular Genetics, Institute for Comprehensive Medical Science, Fujita Health University, 1-98 Dengakugakubo, Kutsukake-cho, Toyoake, Aichi, 470-1192, Japan.
  • Kato A; Division of Molecular Genetics, Institute for Comprehensive Medical Science, Fujita Health University, 1-98 Dengakugakubo, Kutsukake-cho, Toyoake, Aichi, 470-1192, Japan.
  • Kanyama K; Division of Molecular Genetics, Institute for Comprehensive Medical Science, Fujita Health University, 1-98 Dengakugakubo, Kutsukake-cho, Toyoake, Aichi, 470-1192, Japan.
  • Mizuno S; Department of Clinical Genetics, Central Hospital, Aichi Developmental Disability Center, Kasugai, Kasugai, Japan.
  • Muramatsu Y; Department of Pediatrics, Nagoya University Graduate School of Medicine, Nagoya, Japan.
  • Yamamoto T; Institute of Medical Genetics, Tokyo Women's Medical University, Shinjuku, Japan.
  • Shinya M; Genetic Counseling Room, Kagoshima University Hospital, Kagoshima, Japan.
  • Tazaki Y; Department of Obstetrics and Gynecology, Faculty of Medicine, Kagoshima, Japan.
  • Hiwatashi S; Genetic Counseling Room, Kagoshima University Hospital, Kagoshima, Japan.
  • Ikeda T; Department of Obstetrics and Gynecology, Faculty of Medicine, Kagoshima, Japan.
  • Ozaki M; Genetic Counseling Room, Kagoshima University Hospital, Kagoshima, Japan.
  • Kurahashi H; Department of Obstetrics and Gynecology, Faculty of Medicine, Kagoshima, Japan.
Hum Genet ; 139(11): 1417-1427, 2020 Nov.
Article en En | MEDLINE | ID: mdl-32488466
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.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Cromosomas / Eliminación de Secuencia / Duplicación de Gen / Trastornos de los Cromosomas / Inversión Cromosómica Límite: Humans Idioma: En Revista: Hum Genet Año: 2020 Tipo del documento: Article País de afiliación: Japón

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Cromosomas / Eliminación de Secuencia / Duplicación de Gen / Trastornos de los Cromosomas / Inversión Cromosómica Límite: Humans Idioma: En Revista: Hum Genet Año: 2020 Tipo del documento: Article País de afiliación: Japón