دورية أكاديمية

Transcriptome analysis of the zebrafish atoh7−/− Mutant, lakritz, highlights Atoh7‐dependent genetic networks with potential implications for human eye diseases

التفاصيل البيبلوغرافية
العنوان: Transcriptome analysis of the zebrafish atoh7−/− Mutant, lakritz, highlights Atoh7‐dependent genetic networks with potential implications for human eye diseases
المؤلفون: Covello, Giuseppina, Rossello, Fernando J, Filosi, Michele, Gajardo, Felipe, Duchemin, Anne‐Laure, Tremonti, Beatrice F, Eichenlaub, Michael, Polo, Jose M, Powell, David, Ngai, John, Allende, Miguel L, Domenici, Enrico, Ramialison, Mirana, Poggi, Lucia
المصدر: FASEB BioAdvances, vol 2, iss 7
بيانات النشر: eScholarship, University of California
سنة النشر: 2020
المجموعة: University of California: eScholarship
مصطلحات موضوعية: Biological Sciences, Bioinformatics and Computational Biology, Genetics, Neurosciences, Eye Disease and Disorders of Vision, Aetiology, 2.1 Biological and endogenous factors, Eye, Ath5, human retina, inherited eye diseases, retinal ganglion cells, transcriptome analysis
جغرافية الموضوع: 434 - 448
الوصف: Expression of the bHLH transcription protein Atoh7 is a crucial factor conferring competence to retinal progenitor cells for the development of retinal ganglion cells. Several studies have emerged establishing ATOH7 as a retinal disease gene. Remarkably, such studies uncovered ATOH7 variants associated with global eye defects including optic nerve hypoplasia, microphthalmia, retinal vascular disorders, and glaucoma. The complex genetic networks and cellular decisions arising downstream of atoh7 expression, and how their dysregulation cause development of such disease traits remains unknown. To begin to understand such Atoh7-dependent events in vivo, we performed transcriptome analysis of wild-type and atoh7 mutant (lakritz) zebrafish embryos at the onset of retinal ganglion cell differentiation. We investigated in silico interplays of atoh7 and other disease-related genes and pathways. By network reconstruction analysis of differentially expressed genes, we identified gene clusters enriched in retinal development, cell cycle, chromatin remodeling, stress response, and Wnt pathways. By weighted gene coexpression network, we identified coexpression modules affected by the mutation and enriched in retina development genes tightly connected to atoh7. We established the groundwork whereby Atoh7-linked cellular and molecular processes can be investigated in the dynamic multi-tissue environment of the developing normal and diseased vertebrate eye.
نوع الوثيقة: article in journal/newspaper
وصف الملف: application/pdf
اللغة: unknown
العلاقة: qt46r6676z; https://escholarship.org/uc/item/46r6676zTest
الإتاحة: https://escholarship.org/uc/item/46r6676zTest
حقوق: public
رقم الانضمام: edsbas.4DE117DF
قاعدة البيانات: BASE