New regulators of Drosophila eye development identified from temporal transcriptome changes

Author:

Quiquand Manon1,Rimesso Gerard1,Qiao Nan2,Suo Shengbao2,Zhao Chunyu2,Slattery Matthew3,White Kevin P3,Han Jackie J2,Baker Nicholas E145ORCID

Affiliation:

1. Department of Genetics, Albert Einstein College of Medicine, Bronx, NY 10461, USA

2. CAS Key Laboratory of Computational Biology, CAS-MPG Partner Institute for Computational Biology, Shanghai Institute of Nutrition and Health, Chinese Academy of Sciences Center for Excellence in Molecular Cell Science, Collaborative Innovation Center for Genetics and Developmental Biology, Shanghai Institutes for Biological Sciences, Chinese Academy of Sciences, Shanghai 200031, China

3. Institute for Genomics & Systems Biology, University of Chicago, Chicago, IL 60637, USA

4. Department of Ophthalmology and Visual Sciences, Albert Einstein College of Medicine, Bronx, NY 10461, USA

5. Department of Developmental and Molecular Biology, Albert Einstein College of Medicine, Bronx, NY 10461, USA

Abstract

Abstract In the last larval instar, uncommitted progenitor cells in the Drosophila eye primordium start to adopt individual retinal cell fates, arrest their growth and proliferation, and initiate terminal differentiation into photoreceptor neurons and other retinal cell types. To explore the regulation of these processes, we have performed mRNA-Seq studies of the larval eye and antennal primordial at multiple developmental stages. A total of 10,893 fly genes were expressed during these stages and could be adaptively clustered into gene groups, some of whose expression increases or decreases in parallel with the cessation of proliferation and onset of differentiation. Using in situ hybridization of a sample of 98 genes to verify spatial and temporal expression patterns, we estimate that 534 genes or more are transcriptionally upregulated during retinal differentiation, and 1367 or more downregulated as progenitor cells differentiate. Each group of co-expressed genes is enriched for regulatory motifs recognized by co-expressed transcription factors, suggesting that they represent coherent transcriptional regulatory programs. Using available mutant strains, we describe novel roles for the transcription factors SoxNeuro (SoxN), H6-like homeobox (Hmx), CG10253, without children (woc), Structure specific recognition protein (Ssrp), and multisex combs (mxc).

Funder

Chinese Academy of Sciences for a Visiting

National Institutes of Health

National Natural Science Foundation of China

China Ministry of Science and Technology

Analytical Imaging Facility

Albert Einstein College of Medicine

NCI

Publisher

Oxford University Press (OUP)

Subject

Genetics

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