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Published June 18, 2024 | Published
Journal Article Open

Single-tissue proteomics in Caenorhabditis elegans reveals proteins resident in intestinal lysosome-related organelles

Abstract

The nematode intestine is the primary site for nutrient uptake and storage as well as the synthesis of biomolecules; lysosome-related organelles known as gut granules are important for many of these functions. Aspects of intestine biology are not well understood, including the export of the nutrients it imports and the molecules it synthesizes, as well as the complete functions and protein content of the gut granules. Here, we report a mass spectrometry (MS)–based proteomic analysis of the intestine of the Caenorhabditis elegans and of its gut granules. Overall, we identified approximately 5,000 proteins each in the intestine and the gonad and showed that most of these proteins can be detected in samples extracted from a single worm, suggesting the feasibility of individual-level genetic analysis using proteomes. Comparing proteomes and published transcriptomes of the intestine and the gonad, we identified proteins that appear to be synthesized in the intestine and then transferred to the gonad. To identify gut granule proteins, we compared the proteome of individual intestines deficient in gut granules to the wild type. The identified gut granule proteome includes proteins known to be exclusively localized to the granules and additional putative gut granule proteins. We selected two of these putative gut granule proteins for validation via immunohistochemistry, and our successful confirmation of both suggests that our strategy was effective in identifying the gut granule proteome. Our results demonstrate the practicability of single-tissue MS–based proteomic analysis in small organisms and in its future utility.

Copyright and License

© 2024 the Author(s). Published by PNAS. This article is distributed under Creative Commons Attribution-NonCommercial-NoDerivatives License 4.0 (CC BY-NC-ND).

Acknowledgement

We thank members of the Sternberg Lab, the Chou Lab, and the Proteome Exploration Laboratory (PEL) for their discussion and suggestions. We would especially like to thank Hillel Schwartz, Nicholas Markarian, and Mark Zhang for their valuable suggestions and critical reading of the manuscript. We would also like to thank Jeff Jones, Shekufeh Zareian of PEL, and Shan Li of the Chou Lab for their assistance in the preliminary stages of this work, and Wilber Palma, Stephanie Nava, and Barbara Perry of the Sternberg Lab for laboratory assistance. The mutant strain OJ1347 was a gift from Dr. Derek Sieburth of the University of Southern California, Los Angeles, CA 90033. The PEL is supported by the Beckman Institute at Caltech. This research was supported by the Caltech Center for Environmental Microbial Interactions and NIH award R24OD023041 to P.W.S.

Contributions

C.-H.T., T.-Y.W., B.L., T.-F.C., and P.W.S. designed research; C.-H.T., T.-Y.W., H.P., and B.L. performed research; H.P. contributed new reagents/analytic tools; C.-H.T., T.-Y.W., and P.W.S. analyzed data; and C.-H.T., T.-Y.W., T.-F.C., and P.W.S. wrote the paper.

Data Availability

Proteomics data have been deposited in PRIDE (PXD047792) (114).

Conflict of Interest

The authors declare no competing interest.

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Additional details

Created:
June 12, 2024
Modified:
June 12, 2024