An integrated transcriptional analysis of the developing human retina

Author:

Mellough Carla B.12ORCID,Bauer Roman3ORCID,Collin Joseph1ORCID,Dorgau Birthe1,Zerti Darin1,Dolan David W. P.4,Jones Carl M.4,Izuogu Osagie G.15,Yu Min1,Hallam Dean1,Steyn Jannetta S.1,White Kathryn6,Steel David H.1,Santibanez-Koref Mauro1,Elliott David J.1,Jackson Michael S.1,Lindsay Susan1,Grellscheid Sushma4,Lako Majlinda1ORCID

Affiliation:

1. Institute of Genetic Medicine, Newcastle University, Newcastle NE1 3BZ, UK

2. Lions Eye Institute, 2 Verdun Street, Nedlands, Perth, WA 6009, Australia

3. School of Computing, Newcastle University, Newcastle NE4 5TG, UK

4. Department of Biosciences, Durham University, Stockton Road, Durham DH1 3LE, UK

5. European Bioinformatics Institute (EMBL-EBI), Wellcome Genome Campus, Cambridge CB10 1SD, UK

6. EM Research Services, Newcastle University, Newcastle NE2 4HH, UK

Abstract

ABSTRACT The scarcity of embryonic/foetal material as a resource for direct study means that there is still limited understanding of human retina development. Here, we present an integrated transcriptome analysis combined with immunohistochemistry in human eye and retinal samples from 4 to 19 post-conception weeks. This analysis reveals three developmental windows with specific gene expression patterns that informed the sequential emergence of retinal cell types and enabled identification of stage-specific cellular and biological processes, and transcriptional regulators. Each stage is characterised by a specific set of alternatively spliced transcripts that code for proteins involved in the formation of the photoreceptor connecting cilium, pre-mRNA splicing and epigenetic modifiers. Importantly, our data show that the transition from foetal to adult retina is characterised by a large increase in the percentage of mutually exclusive exons that code for proteins involved in photoreceptor maintenance. The circular RNA population is also defined and shown to increase during retinal development. Collectively, these data increase our understanding of human retinal development and the pre-mRNA splicing process, and help to identify new candidate disease genes.

Funder

European Research Council

Medical Research Council

Fight for Sight

Biotechnology and Biological Sciences Research Council

Macular Society

RP Fighting Blindness

Leverhulme Trust

Wellcome Trust

Engineering and Physical Sciences Research Council

Publisher

The Company of Biologists

Subject

Developmental Biology,Molecular Biology

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