FuncPEP v2.0: An Updated Database of Functional Short Peptides Translated from Non-Coding RNAs

Author:

Mohapatra Swati12,Banerjee Anik23,Rausseo Paola14,Dragomir Mihnea P.567ORCID,Manyam Ganiraju C.8,Broom Bradley M.8,Calin George A.19ORCID

Affiliation:

1. Department of Translational Molecular Pathology, University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA

2. The University of Texas MD Anderson Cancer Center UTHealth Houston Graduate School of Biomedical Sciences, Houston, TX 77030, USA

3. Department of Neurology, University of Texas McGovern Medical School, Houston, TX 77030, USA

4. Scripps College, Claremont, CA 91711, USA

5. Institute of Pathology, Charité—Universitätsmedizin Berlin, Corporate Member of Freie Universität Berlin and Humboldt-Universität zu Berlin, 10117 Berlin, Germany

6. German Cancer Consortium (DKTK), German Cancer Research Center (DKFZ), 69120 Heidelberg, Germany

7. Berlin Institute of Health at Charité, 10117 Berlin, Germany

8. Department of Bioinformatics and Computational Biology, The University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA

9. Center for RNA Interference and Non-Coding RNAs, The University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA

Abstract

Over the past decade, there have been reports of short novel functional peptides (less than 100 aa in length) translated from so-called non-coding RNAs (ncRNAs) that have been characterized using mass spectrometry (MS) and large-scale proteomics studies. Therefore, understanding the bivalent functions of some ncRNAs as transcripts that encode both functional RNAs and short peptides, which we named ncPEPs, will deepen our understanding of biology and disease. In 2020, we published the first database of functional peptides translated from non-coding RNAs—FuncPEP. Herein, we have performed an update including the newly published ncPEPs from the last 3 years along with the categorization of host ncRNAs. FuncPEP v2.0 contains 152 functional ncPEPs, out of which 40 are novel entries. A PubMed search from August 2020 to July 2023 incorporating specific keywords was performed and screened for publications reporting validated functional peptides derived from ncRNAs. We did not observe a significant increase in newly discovered functional ncPEPs, but a steady increase. The novel identified ncPEPs included in the database were characterized by a wide array of molecular and physiological parameters (i.e., types of host ncRNA, species distribution, chromosomal density, distribution of ncRNA length, identification methods, molecular weight, and functional distribution across humans and other species). We consider that, despite the fact that MS can now easily identify ncPEPs, there still are important limitations in proving their functionality.

Funder

NCI

NIGMS

DoD

Chronic Lymphocytic Leukemia Moonshot Flagship project

CLL Global Research Foundation

G. Harold & Leila Y. Mathers Foundation

Torrey Coast Foundation

Brain SPORE

Cancer Prevention and Research Institute of Texas

Schissler Foundation Fellowship

Andrew Sowell-Wade Huggins Scholarship in Cancer Research

Steve Lasher and Janiece Longoria Graduate Student Research Award

SIC Academic Achievement

American Heart Association (AHA) National Predoctoral Fellowship

John J. Kopchick Research Award

Jesse B. Heath, Jr. Family Legacy Award

Partnership for Careers in Cancer Science and Medicine

Berlin Institute of Health

DKTK Berlin

NIH/NCI

Publisher

MDPI AG

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