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The New England journal of medicine · 2018

Essential Role of BRCA2 in Ovarian Development and Function.

Клинический случайСтатьяПоддержка исследования: вне правительства СШАНазвание и аннотация: Перевод в очереди
Обработка статьи · этапы, ошибки и управление
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Weinberg-Shukron Ariella, Rachmiel Mariana, Renbaum Paul, Gulsuner Suleyman, Walsh Tom, Lobel Orit, Dreifuss Amatzia, Ben-Moshe Avital, Zeligson Sharon, Segel Reeval, Shore Tikva, Kalifa Rachel, Goldberg Michal, King Mary-Claire, Gerlitz Offer, Levy-Lahad Ephrat, Zangen David

Аннотация

The causes of ovarian dysgenesis remain incompletely understood. Two sisters with XX ovarian dysgenesis carried compound heterozygous truncating mutations in the BRCA2 gene that led to reduced BRCA2 protein levels and an impaired response to DNA damage, which resulted in chromosomal breakage and the failure of RAD51 to be recruited to double-stranded DNA breaks. The sisters also had microcephaly, and one sister was in long-term remission from leukemia, which had been diagnosed when she was 5 years old. Drosophila mutants that were null for an orthologue of BRCA2 were sterile, and gonadal dysgenesis was present in both sexes. These results revealed a new role for BRCA2 and highlight the importance to ovarian development of genes that are critical for recombination during meiosis. (Funded by the Israel Science Foundation and others.).

Предметные рубрики MeSH

ИП Урсолов Владлен Сергеевич

ИНН 500118482352 · ОГРНИП 314500117700049

Реквизиты и контакты