Identification of a heterogeneous and dynamic ciliome during embryonic development and cell differentiation

Author:

Elliott Kelsey H.12,Balchand Sai K.2,Bonatto Paese Christian Louis12ORCID,Chang Ching-Fang12,Yang Yanfen12,Brown Kari M.12,Rasicci Daniel T.3,He Hao3,Thorner Konrad1,Chaturvedi Praneet1,Murray Stephen A.3,Chen Jing24ORCID,Porollo Aleksey245,Peterson Kevin A.3ORCID,Brugmann Samantha A.126ORCID

Affiliation:

1. Cincinnati Children's Hospital Medical 1 Division of Developmental Biology, Department of Pediatrics , , Cincinnati, OH 45229 , USA

2. University of Cincinnati, College of Medicine 2 , Department of Pediatrics, Cincinnati, OH 45229 , USA

3. The Jackson Laboratory 3 , Bar Harbor, ME 04609 , USA

4. Cincinnati Children's Hospital Medical 4 Division of Biomedical Informatics , , Cincinnati, OH 45229 , USA

5. Center for Autoimmune Genomics and Etiology, Cincinnati Children's Hospital Medical 5 , Cincinnati, OH 45229 , USA

6. Cincinnati Children's Hospital Medical Center 6 Division of Plastic Surgery, Department of Surgery , , Cincinnati, OH 45229 , USA

Abstract

ABSTRACT Primary cilia are nearly ubiquitous organelles that transduce molecular and mechanical signals. Although the basic structure of the cilium and the cadre of genes that contribute to ciliary formation and function (the ciliome) are believed to be evolutionarily conserved, the presentation of ciliopathies with narrow, tissue-specific phenotypes and distinct molecular readouts suggests that an unappreciated heterogeneity exists within this organelle. Here, we provide a searchable transcriptomic resource for a curated primary ciliome, detailing various subgroups of differentially expressed genes within the ciliome that display tissue and temporal specificity. Genes within the differentially expressed ciliome exhibited a lower level of functional constraint across species, suggesting organism and cell-specific function adaptation. The biological relevance of ciliary heterogeneity was functionally validated by using Cas9 gene-editing to disrupt ciliary genes that displayed dynamic gene expression profiles during osteogenic differentiation of multipotent neural crest cells. Collectively, this novel primary cilia-focused resource will allow researchers to explore longstanding questions related to how tissue and cell-type specific functions and ciliary heterogeneity may contribute to the range of phenotypes associated with ciliopathies.

Funder

National Institute of General Medical Sciences

National Institutes of Health

National Institute of Dental and Craniofacial Research

Publisher

The Company of Biologists

Subject

Developmental Biology,Molecular Biology

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