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Evidence of natural selection in the mitochondrial-derived peptides humanin and SHLP6
Mitochondrial-derived peptides are encoded by mitochondrial DNA but have biological activity outside mitochondria. Eight of these are encoded by sequences within the mitochondrial 12S and 16S ribosomal genes: humanin, MOTS-c, and the six SHLP peptides, SHLP1-SHLP6. These peptides have various effect...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10465549/ https://www.ncbi.nlm.nih.gov/pubmed/37644144 http://dx.doi.org/10.1038/s41598-023-41053-0 |
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author | Gruschus, James M. Morris, Daniel L. Tjandra, Nico |
author_facet | Gruschus, James M. Morris, Daniel L. Tjandra, Nico |
author_sort | Gruschus, James M. |
collection | PubMed |
description | Mitochondrial-derived peptides are encoded by mitochondrial DNA but have biological activity outside mitochondria. Eight of these are encoded by sequences within the mitochondrial 12S and 16S ribosomal genes: humanin, MOTS-c, and the six SHLP peptides, SHLP1-SHLP6. These peptides have various effects in cell culture and animal models, affecting neuroprotection, insulin sensitivity, and apoptosis, and some are secreted, potentially having extracellular signaling roles. However, except for humanin, their importance in normal cell function is unknown. To gauge their importance, their coding sequences in vertebrates have been analyzed for synonymous codon bias. Because they lie in RNA genes, such bias should only occur if their amino acids have been conserved to maintain biological function. Humanin and SHLP6 show strong synonymous codon bias and sequence conservation. In contrast, SHLP1, SHLP2, SHLP3, and SHLP5 show no significant bias and are poorly conserved. MOTS-c and SHLP4 also lack significant bias, but contain highly conserved N-terminal regions, and their biological importance cannot be ruled out. An additional potential mitochondrial-derived peptide sequence was discovered preceding SHLP2, named SHLP2b, which also contains a highly conserved N-terminal region with synonymous codon bias. |
format | Online Article Text |
id | pubmed-10465549 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-104655492023-08-31 Evidence of natural selection in the mitochondrial-derived peptides humanin and SHLP6 Gruschus, James M. Morris, Daniel L. Tjandra, Nico Sci Rep Article Mitochondrial-derived peptides are encoded by mitochondrial DNA but have biological activity outside mitochondria. Eight of these are encoded by sequences within the mitochondrial 12S and 16S ribosomal genes: humanin, MOTS-c, and the six SHLP peptides, SHLP1-SHLP6. These peptides have various effects in cell culture and animal models, affecting neuroprotection, insulin sensitivity, and apoptosis, and some are secreted, potentially having extracellular signaling roles. However, except for humanin, their importance in normal cell function is unknown. To gauge their importance, their coding sequences in vertebrates have been analyzed for synonymous codon bias. Because they lie in RNA genes, such bias should only occur if their amino acids have been conserved to maintain biological function. Humanin and SHLP6 show strong synonymous codon bias and sequence conservation. In contrast, SHLP1, SHLP2, SHLP3, and SHLP5 show no significant bias and are poorly conserved. MOTS-c and SHLP4 also lack significant bias, but contain highly conserved N-terminal regions, and their biological importance cannot be ruled out. An additional potential mitochondrial-derived peptide sequence was discovered preceding SHLP2, named SHLP2b, which also contains a highly conserved N-terminal region with synonymous codon bias. Nature Publishing Group UK 2023-08-29 /pmc/articles/PMC10465549/ /pubmed/37644144 http://dx.doi.org/10.1038/s41598-023-41053-0 Text en © This is a U.S. Government work and not under copyright protection in the US; foreign copyright protection may apply 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Gruschus, James M. Morris, Daniel L. Tjandra, Nico Evidence of natural selection in the mitochondrial-derived peptides humanin and SHLP6 |
title | Evidence of natural selection in the mitochondrial-derived peptides humanin and SHLP6 |
title_full | Evidence of natural selection in the mitochondrial-derived peptides humanin and SHLP6 |
title_fullStr | Evidence of natural selection in the mitochondrial-derived peptides humanin and SHLP6 |
title_full_unstemmed | Evidence of natural selection in the mitochondrial-derived peptides humanin and SHLP6 |
title_short | Evidence of natural selection in the mitochondrial-derived peptides humanin and SHLP6 |
title_sort | evidence of natural selection in the mitochondrial-derived peptides humanin and shlp6 |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10465549/ https://www.ncbi.nlm.nih.gov/pubmed/37644144 http://dx.doi.org/10.1038/s41598-023-41053-0 |
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