دورية أكاديمية

Functional study on new FOXL2 mutations found in Chinese patients with blepharophimosis, ptosis, epicanthus inversus syndrome

التفاصيل البيبلوغرافية
العنوان: Functional study on new FOXL2 mutations found in Chinese patients with blepharophimosis, ptosis, epicanthus inversus syndrome
المؤلفون: Lu Zhou, Jiaqi Wang, Tailing Wang
المصدر: BMC Medical Genetics, Vol 19, Iss 1, Pp 1-7 (2018)
بيانات النشر: BMC, 2018.
سنة النشر: 2018
المجموعة: LCC:Internal medicine
LCC:Genetics
مصطلحات موضوعية: BPES, FOXL2, Gene mutation, Internal medicine, RC31-1245, Genetics, QH426-470
الوصف: Abstract Background Blepharophimosis, ptosis, epicanthus inversus syndrome (BPES) is a rare inheritable disease that mainly affects eyelid development associated with (type I) or without (type II) ovarian dysfunction, resulting in premature ovarian failure (POF). Mutations in the gene forkhead box L2 (FOXL2) have been shown to be responsible for BPES. The aim of this study was to determine and functionally validate the FOXL2 mutation in a Chinese BPES family. Methods Twelve individuals including five BPES patients from a Chinese family were enrolled. Genomic DNA was extracted from peripheral blood of enrolled subjects. The coding region of the FOXL2 gene was amplified and mutations were determined by sequencing analyses. Functional analysis was carried out to study changes in expression and transcriptional activity of the mutant FOXL2 protein. Results A novel mutation in the FOXL2 gene (c.931C > T) was detected in all five BPES patients, which converts a histidine residue into a tyrosine (p.H311Y) in the FOXL2 protein. Functional analysis revealed that this point mutation reduces FOXL2 protein expression, concomitant with decreased transcriptional activity on the steroidogenic acute regulatory (StAR) gene promotor. Conclusions Our results expand the mutational spectrum of the FOXL2 gene and provide additional insights to the research on the molecular pathogenesis of FOXL2 in BPES.
نوع الوثيقة: article
وصف الملف: electronic resource
اللغة: English
تدمد: 1471-2350
Relation: http://link.springer.com/article/10.1186/s12881-018-0631-8; https://doaj.org/toc/1471-2350
DOI: 10.1186/s12881-018-0631-8
URL الوصول: https://doaj.org/article/a5fa673115674e6c96d74f249faa4e59
رقم الأكسشن: edsdoj.5fa673115674e6c96d74f249faa4e59
قاعدة البيانات: Directory of Open Access Journals
الوصف
تدمد:14712350
DOI:10.1186/s12881-018-0631-8