Summary of Study ST002162

This data is available at the NIH Common Fund's National Metabolomics Data Repository (NMDR) website, the Metabolomics Workbench, https://www.metabolomicsworkbench.org, where it has been assigned Project ID PR001375. The data can be accessed directly via it's Project DOI: 10.21228/M8069C This work is supported by NIH grant, U2C- DK119886.

See: https://www.metabolomicsworkbench.org/about/howtocite.php

This study contains a large results data set and is not available in the mwTab file. It is only available for download via FTP as data file(s) here.

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Study IDST002162
Study TitleCFAP418 participates in membrane-associated cellular processes through binding lipids during ciliogenesis
Study SummaryCiliopathies and retinal degenerative diseases are heterogeneous groups of genetic diseases. CFAP418 is a causative gene of both diseases, and its sequence is evolutionarily conserved. Here, we employ affinity purification coupled with mass spectrometry and quantitative lipidomic, proteomic, and phosphoproteomic approaches to address the function of CFAP418 in retinas. We show CFAP418 unexpectedly binds to lipid metabolism precursor phosphatidic acid (PA) and mitochondrion-specific lipid cardiolipin but does not form a tight and static complex with proteins. Loss of Cfap418 leads to a widespread disruption of membrane lipid homeostasis and changes in protein-membrane association, which subsequently causes mitochondrial morphological and functional defects and membrane remodeling abnormalities in multiple vesicular trafficking pathways. The signaling of PA-binding protein kinase Ca is increased. Our results indicate that membrane lipid imbalance is a new pathological mechanism underlying inherited ciliopathies and retinal degenerations, which is associated with other known causative RAB28 and BBS genes.
Institute
University of Utah - Metabolomics Core
Last NameMaschek
First NameJohn
AddressEmma Eccles Jones Medical Science Building, 15 N Medical Dr East, Salt Lake City, UT, 84112, USA
Emailalan.maschek@pharm.utah.edu
Phone801-587-7779
Submit Date2022-05-10
Raw Data AvailableYes
Raw Data File Type(s)mzML
Analysis Type DetailLC-MS
Release Date2023-05-10
Release Version1
John Maschek John Maschek
https://dx.doi.org/10.21228/M8069C
ftp://www.metabolomicsworkbench.org/Studies/ application/zip

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Factors:

Subject type: Mammal; Subject species: Mus musculus (Factor headings shown in green)

mb_sample_id local_sample_id Factor
SA20749124Het
SA20749222Het
SA20749326Het
SA20749429Het
SA20749521Het
SA20749630Het
SA20749728Het
SA20749823Het
SA20749916Het
SA20750015Het
SA2075017Het
SA2075025Het
SA20750313Het
SA2075042Het
SA20750519Het
SA20750612Het
SA2075079KO
SA2075088KO
SA2075096KO
SA2075103KO
SA2075114KO
SA20751210KO
SA20751314KO
SA20751418KO
SA20751525KO
SA2075161KO
SA20751727KO
SA20751817KO
SA20751920KO
SA20752037KO
SA20752131KO
SA20752211KO
SA207479blank 03#N/A
SA207480pooledQC 01#N/A
SA207481blank 02#N/A
SA207482blank 01#N/A
SA207483blank 00#N/A
SA207484pooledQC 02#N/A
SA207485pooledQC 00#N/A
SA207486pooledQC 06#N/A
SA207487pooledQC 03#N/A
SA207488pooledQC 05#N/A
SA207489pooledQC 07#N/A
SA207490pooledQC 04#N/A
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