Cargando…
Strong Selectional Forces Fine-Tune CpG Content in Genes Involved in Neurological Disorders as Revealed by Codon Usage Patterns
Neurodegenerative disorders cause irreversible damage to the neurons and adversely affect the quality of life. Protein misfolding and their aggregation in specific parts of the brain, mitochondrial dysfunction, calcium load, proteolytic stress, and oxidative stress are among the causes of neurodegen...
Autores principales: | , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9226491/ https://www.ncbi.nlm.nih.gov/pubmed/35757545 http://dx.doi.org/10.3389/fnins.2022.887929 |
_version_ | 1784733892891115520 |
---|---|
author | Khandia, Rekha Sharma, Anushri Alqahtani, Taha Alqahtani, Ali M. Asiri, Yahya I. Alqahtani, Saud Alharbi, Ahmed M. Kamal, Mohammad Amjad |
author_facet | Khandia, Rekha Sharma, Anushri Alqahtani, Taha Alqahtani, Ali M. Asiri, Yahya I. Alqahtani, Saud Alharbi, Ahmed M. Kamal, Mohammad Amjad |
author_sort | Khandia, Rekha |
collection | PubMed |
description | Neurodegenerative disorders cause irreversible damage to the neurons and adversely affect the quality of life. Protein misfolding and their aggregation in specific parts of the brain, mitochondrial dysfunction, calcium load, proteolytic stress, and oxidative stress are among the causes of neurodegenerative disorders. In addition, altered metabolism has been associated with neurodegeneration as evidenced by reductions in glutamine and alanine in transient global amnesia patients, higher homocysteine-cysteine disulfide, and lower methionine decline in serum urea have been observed in Alzheimer’s disease patients. Neurodegeneration thus appears to be a culmination of altered metabolism. The study’s objective is to analyze various attributes like composition, physical properties of the protein, and factors like selectional and mutational forces, influencing codon usage preferences in a panel of genes involved directly or indirectly in metabolism and contributing to neurodegeneration. Various parameters, including gene composition, dinucleotide analysis, Relative synonymous codon usage (RSCU), Codon adaptation index (CAI), neutrality and parity plots, and different protein indices, were computed and analyzed to determine the codon usage pattern and factors affecting it. The correlation of intrinsic protein properties such as the grand average of hydropathicity index (GRAVY), isoelectric point, hydrophobicity, and acidic, basic, and neutral amino acid content has been found to influence codon usage. In genes up to 800 amino acids long, the GC3 content was highly variable, while GC12 content was relatively constant. An optimum CpG content is present in genes to maintain a high expression level as required for genes involved in metabolism. Also observed was a low codon usage bias with a higher protein expression level. Compositional parameters and nucleotides at the second position of codons played essential roles in explaining the extent of bias. Overall analysis indicated that the dominance of selection pressure and compositional constraints and mutational forces shape codon usage. |
format | Online Article Text |
id | pubmed-9226491 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-92264912022-06-25 Strong Selectional Forces Fine-Tune CpG Content in Genes Involved in Neurological Disorders as Revealed by Codon Usage Patterns Khandia, Rekha Sharma, Anushri Alqahtani, Taha Alqahtani, Ali M. Asiri, Yahya I. Alqahtani, Saud Alharbi, Ahmed M. Kamal, Mohammad Amjad Front Neurosci Neuroscience Neurodegenerative disorders cause irreversible damage to the neurons and adversely affect the quality of life. Protein misfolding and their aggregation in specific parts of the brain, mitochondrial dysfunction, calcium load, proteolytic stress, and oxidative stress are among the causes of neurodegenerative disorders. In addition, altered metabolism has been associated with neurodegeneration as evidenced by reductions in glutamine and alanine in transient global amnesia patients, higher homocysteine-cysteine disulfide, and lower methionine decline in serum urea have been observed in Alzheimer’s disease patients. Neurodegeneration thus appears to be a culmination of altered metabolism. The study’s objective is to analyze various attributes like composition, physical properties of the protein, and factors like selectional and mutational forces, influencing codon usage preferences in a panel of genes involved directly or indirectly in metabolism and contributing to neurodegeneration. Various parameters, including gene composition, dinucleotide analysis, Relative synonymous codon usage (RSCU), Codon adaptation index (CAI), neutrality and parity plots, and different protein indices, were computed and analyzed to determine the codon usage pattern and factors affecting it. The correlation of intrinsic protein properties such as the grand average of hydropathicity index (GRAVY), isoelectric point, hydrophobicity, and acidic, basic, and neutral amino acid content has been found to influence codon usage. In genes up to 800 amino acids long, the GC3 content was highly variable, while GC12 content was relatively constant. An optimum CpG content is present in genes to maintain a high expression level as required for genes involved in metabolism. Also observed was a low codon usage bias with a higher protein expression level. Compositional parameters and nucleotides at the second position of codons played essential roles in explaining the extent of bias. Overall analysis indicated that the dominance of selection pressure and compositional constraints and mutational forces shape codon usage. Frontiers Media S.A. 2022-06-10 /pmc/articles/PMC9226491/ /pubmed/35757545 http://dx.doi.org/10.3389/fnins.2022.887929 Text en Copyright © 2022 Khandia, Sharma, Alqahtani, Alqahtani, Asiri, Alqahtani, Alharbi and Kamal. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Neuroscience Khandia, Rekha Sharma, Anushri Alqahtani, Taha Alqahtani, Ali M. Asiri, Yahya I. Alqahtani, Saud Alharbi, Ahmed M. Kamal, Mohammad Amjad Strong Selectional Forces Fine-Tune CpG Content in Genes Involved in Neurological Disorders as Revealed by Codon Usage Patterns |
title | Strong Selectional Forces Fine-Tune CpG Content in Genes Involved in Neurological Disorders as Revealed by Codon Usage Patterns |
title_full | Strong Selectional Forces Fine-Tune CpG Content in Genes Involved in Neurological Disorders as Revealed by Codon Usage Patterns |
title_fullStr | Strong Selectional Forces Fine-Tune CpG Content in Genes Involved in Neurological Disorders as Revealed by Codon Usage Patterns |
title_full_unstemmed | Strong Selectional Forces Fine-Tune CpG Content in Genes Involved in Neurological Disorders as Revealed by Codon Usage Patterns |
title_short | Strong Selectional Forces Fine-Tune CpG Content in Genes Involved in Neurological Disorders as Revealed by Codon Usage Patterns |
title_sort | strong selectional forces fine-tune cpg content in genes involved in neurological disorders as revealed by codon usage patterns |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9226491/ https://www.ncbi.nlm.nih.gov/pubmed/35757545 http://dx.doi.org/10.3389/fnins.2022.887929 |
work_keys_str_mv | AT khandiarekha strongselectionalforcesfinetunecpgcontentingenesinvolvedinneurologicaldisordersasrevealedbycodonusagepatterns AT sharmaanushri strongselectionalforcesfinetunecpgcontentingenesinvolvedinneurologicaldisordersasrevealedbycodonusagepatterns AT alqahtanitaha strongselectionalforcesfinetunecpgcontentingenesinvolvedinneurologicaldisordersasrevealedbycodonusagepatterns AT alqahtanialim strongselectionalforcesfinetunecpgcontentingenesinvolvedinneurologicaldisordersasrevealedbycodonusagepatterns AT asiriyahyai strongselectionalforcesfinetunecpgcontentingenesinvolvedinneurologicaldisordersasrevealedbycodonusagepatterns AT alqahtanisaud strongselectionalforcesfinetunecpgcontentingenesinvolvedinneurologicaldisordersasrevealedbycodonusagepatterns AT alharbiahmedm strongselectionalforcesfinetunecpgcontentingenesinvolvedinneurologicaldisordersasrevealedbycodonusagepatterns AT kamalmohammadamjad strongselectionalforcesfinetunecpgcontentingenesinvolvedinneurologicaldisordersasrevealedbycodonusagepatterns |