Human genetics · 2014
Homozygous truncating PTPRF mutation causes athelia.
СтатьяНазвание и аннотация: Перевод в очереди
Обработка статьи · этапы, ошибки и управление
Загрузка состояния…
Ошибки и ограничения
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.
Borck Guntram, de Vries Liat, Wu Hsin-Jung, Smirin-Yosef Pola, Nürnberg Gudrun, Lagovsky Irina, Ishida Luis Henrique, Thierry Patrick, Wieczorek Dagmar, Nürnberg Peter, Foley John, Kubisch Christian, Basel-Vanagaite Lina
Аннотация
Athelia is a very rare entity that is defined by the absence of the nipple-areola complex. It can affect either sex and is mostly part of syndromes including other congenital or ectodermal anomalies, such as limb-mammary syndrome, scalp-ear-nipple syndrome, or ectodermal dysplasias. Here, we report on three children from two branches of an extended consanguineous Israeli Arab family, a girl and two boys, who presented with a spectrum of nipple anomalies ranging from unilateral hypothelia to bilateral athelia but no other consistently associated anomalies except a characteristic eyebrow shape. Using homozygosity mapping after single nucleotide polymorphism (SNP) array genotyping and candidate gene sequencing we identified a homozygous frameshift mutation in PTPRF as the likely cause of nipple anomalies in this family. PTPRF encodes a receptor-type protein phosphatase that localizes to adherens junctions and may be involved in the regulation of epithelial cell-cell contacts, peptide growth factor signaling, and the canonical Wnt pathway. Together with previous reports on female mutant Ptprf mice, which have a lactation defect, and disruption of one allele of PTPRF by a balanced translocation in a woman with amastia, our results indicate a key role for PTPRF in the development of the nipple-areola region.
Предметные рубрики MeSH
AdolescentAdultAnimalsBreastBreast DiseasesCells, CulturedChildChild, PreschoolCongenital AbnormalitiesFemaleFibroblastsFrameshift MutationGene Expression ProfilingGenome-Wide Association StudyHomozygoteHumansInfantMaleMiceNipplesPedigreePolymorphism, Single NucleotideReceptor-Like Protein Tyrosine Phosphatases, Class 2