MedElevator Войти в исследования
← Поиск публикаций

DOI 10.1016/j.ajhg.2013.03.021

Медицинская библиотека · American journal of human genetics · 2013

ZC4H2 mutations are associated with arthrogryposis multiplex congenita and intellectual disability through impairment of central and peripheral synaptic plasticity.

Hirata Hiromi, Nanda Indrajit, van Riesen Anne, McMichael Gai, Hu Hao, Hambrock Melanie, Papon Marie-Amélie, Fischer Ute, Marouillat Sylviane, Ding Can, Alirol Servane, Bienek Melanie, Preisler-Adams Sabine, Grimme Astrid, Seelow Dominik, Webster Richard, Haan Eric, MacLennan Alastair, Stenzel Werner, Yap Tzu Ying, Gardner Alison, Nguyen Lam Son, Shaw Marie, Lebrun Nicolas, Haas Stefan A, Kress Wolfram, Haaf Thomas, Schellenberger Elke, Chelly Jamel, Viot Géraldine, Shaffer Lisa G, Rosenfeld Jill A, Kramer Nancy, Falk Rena, El-Khechen Dima, Escobar Luis F, Hennekam Raoul, Wieacker Peter, Hübner Christoph, Ropers Hans-Hilger, Gecz Jozef, Schuelke Markus, Laumonnier Frédéric, Kalscheuer Vera M

СтатьяПоддержка исследования: вне правительства СШАПеревод в очереди

Аннотация

Arthrogryposis multiplex congenita (AMC) is caused by heterogeneous pathologies leading to multiple antenatal joint contractures through fetal akinesia. Understanding the pathophysiology of this disorder is important for clinical care of the affected individuals and genetic counseling of the families. We thus aimed to establish the genetic basis of an AMC subtype that is associated with multiple dysmorphic features and intellectual disability (ID). We used haplotype analysis, next-generation sequencing, array comparative genomic hybridization, and chromosome breakpoint mapping to identify the pathogenic mutations in families and simplex cases. Suspected disease variants were verified by cosegregation analysis. We identified disease-causing mutations in the zinc-finger gene ZC4H2 in four families affected by X-linked AMC plus ID and one family affected by cerebral palsy. Several heterozygous females were also affected, but to a lesser degree. Furthermore, we found two ZC4H2 deletions and one rearrangement in two female and one male unrelated simplex cases, respectively. In mouse primary hippocampal neurons, transiently produced ZC4H2 localized to the postsynaptic compartment of excitatory synapses, and the altered protein influenced dendritic spine density. In zebrafish, antisense-morpholino-mediated zc4h2 knockdown caused abnormal swimming and impaired α-motoneuron development. All missense mutations identified herein failed to rescue the swimming defect of zebrafish morphants. We conclude that ZC4H2 point mutations, rearrangements, and small deletions cause a clinically variable broad-spectrum neurodevelopmental disorder of the central and peripheral nervous systems in both familial and simplex cases of both sexes. Our results highlight the importance of ZC4H2 for genetic testing of individuals presenting with ID plus muscle weakness and minor or major forms of AMC.

Для цитирования: Hirata Hiromi, Nanda Indrajit, van Riesen Anne, McMichael Gai, Hu Hao, Hambrock Melanie, Papon Marie-Amélie, Fischer Ute, Marouillat Sylviane, Ding Can, Alirol Servane, Bienek Melanie, Preisler-Adams Sabine, Grimme Astrid, Seelow Dominik, Webster Richard, Haan Eric, MacLennan Alastair, Stenzel Werner, Yap Tzu Ying, Gardner Alison, Nguyen Lam Son, Shaw Marie, Lebrun Nicolas, Haas Stefan A, Kress Wolfram, Haaf Thomas, Schellenberger Elke, Chelly Jamel, Viot Géraldine, Shaffer Lisa G, Rosenfeld Jill A, Kramer Nancy, Falk Rena, El-Khechen Dima, Escobar Luis F, Hennekam Raoul, Wieacker Peter, Hübner Christoph, Ropers Hans-Hilger, Gecz Jozef, Schuelke Markus, Laumonnier Frédéric, Kalscheuer Vera M. ZC4H2 mutations are associated with arthrogryposis multiplex congenita and intellectual disability through impairment of central and peripheral synaptic plasticity.. American journal of human genetics. 2013. DOI: 10.1016/j.ajhg.2013.03.021.

Предметные рубрики MeSH

Подготовка и перевод публикации
Обработка статьи · этапы, ошибки и управление
Загрузка состояния…

История · было → стало

Состояние обновляется каждые 5 секунд, пока блок открыт. Процент показывается только там, где известен объём работы. Пауза останавливает продолжение этапа; текущий запрос к источнику может завершиться.

Тип публикации указан по данным источника. Уровень доказательности автоматически не присваивается.