We discovered a novel family of atypical secretory pathway kinases that phosphorylate secreted proteins. One of these kinases, Fam20C, targets SxE/pS motifs on secreted proteins. Approximately 75% of human serum, plasma and cerebrospinal fluid phosphoproteins are phosphorylated on the Fam20C consensus motif, underscoring the importance of this discovery. We used comparative phosphoproteomics to identify over 100 secreted substrates of Fam20C, demonstrating that Fam20C generates the majority of the secreted phosphoproteome. While Fam20C plays a critical role in tissue mineralization, the presence of Fam20C in invertebrates that lack mineralized tissue, as well as the diverse functions of Fam20C substrates, suggest that this kinase has additional roles. Notably, one ancestral substrate of Fam20C is egg yolk vitegllogenin, a secreted phosphoprotein of the Large Lipid Transport Protein (LLTP) family. While vitellogenins are unique to egg-laying animals, LLTP proteins in humans have central roles in lipid transport and include the apolipoproteins and the microsomal triglyceride transfer protein. We found that five human apolipoproteins, APOA2, APOB, APOE, APOL1 and APOA5, as well as proprotein convertase subtilisin type 9 (PCSK9) are all substrates of Fam20C in humans. These results lead us to hypothesize that regulation of lipid trafficking may be one of the major, and possibly the ancestral function of Fam20C. We will test this hypothesis through in vitro and in vivo experiments to establish direct kinase-substrate relationships between Fam20C and PCSK9 or lipoproteins. We will use cell- based assays to specifically study how phosphorylation affects the secretion, processing, and biological activity of these substrates. We have developed a liver-specific Fam20C knockout mouse and will undertake an unbiased mass spectrometry-based lipidomics approach to determine the in vivo contribution of Fam20C to lipid homeostasis. The biological mechanisms responsible for distribution of lipids throughout the body are of fundamental importance to human health and disease, including the massive public health burden of atherosclerosis and heart disease.

Public Health Relevance

Elevated blood cholesterol drives pathological processes like atherosclerosis and heart disease, the leading cause of death in the United States. To confront this public health threat, it is imperative to elucidate the underlying biological processes that regulate lipid trafficking. We have discovered an atypical secreted kinase, Fam20C, that phosphorylates human lipoproteins and PCSK9 in the extracellular space and may orchestrate a novel mechanism of regulating human lipid metabolism.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Individual Predoctoral NRSA for M.D./Ph.D. Fellowships (ADAMHA) (F30)
Project #
5F30HL143859-03
Application #
10077349
Study Section
Special Emphasis Panel (ZRG1)
Program Officer
Meadows, Tawanna
Project Start
2018-12-01
Project End
2021-09-30
Budget Start
2020-12-01
Budget End
2021-09-30
Support Year
3
Fiscal Year
2021
Total Cost
Indirect Cost
Name
University of Texas Sw Medical Center Dallas
Department
Type
Schools of Medicine
DUNS #
800771545
City
Dallas
State
TX
Country
United States
Zip Code
75390