Cargando…
Comparative genome analysis of three euplotid protists provides insights into the evolution of nanochromosomes in unicellular eukaryotic organisms
One of the most diverse clades of ciliated protozoa, the class Spirotrichea, displays a series of unique characters in terms of eukaryotic macronuclear (MAC) genome, including high fragmentation that produces nanochromosomes. However, the genomic diversity and evolution of nanochromosomes and gene f...
Autores principales: | , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Nature Singapore
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10449743/ https://www.ncbi.nlm.nih.gov/pubmed/37637252 http://dx.doi.org/10.1007/s42995-023-00175-0 |
_version_ | 1785095026123997184 |
---|---|
author | Jin, Didi Li, Chao Chen, Xiao Byerly, Adam Stover, Naomi A. Zhang, Tengteng Shao, Chen Wang, Yurui |
author_facet | Jin, Didi Li, Chao Chen, Xiao Byerly, Adam Stover, Naomi A. Zhang, Tengteng Shao, Chen Wang, Yurui |
author_sort | Jin, Didi |
collection | PubMed |
description | One of the most diverse clades of ciliated protozoa, the class Spirotrichea, displays a series of unique characters in terms of eukaryotic macronuclear (MAC) genome, including high fragmentation that produces nanochromosomes. However, the genomic diversity and evolution of nanochromosomes and gene families for spirotrich MAC genomes are poorly understood. In this study, we assemble the MAC genome of a representative euplotid (a new model organism in Spirotrichea) species, Euplotes aediculatus. Our results indicate that: (a) the MAC genome includes 35,465 contigs with a total length of 97.3 Mb and a contig N50 of 3.4 kb, and contains 13,145 complete nanochromosomes and 43,194 predicted genes, with the majority of these nanochromosomes containing tiny introns and harboring only one gene; (b) genomic comparisons between E. aediculatus and other reported spirotrichs indicate that average GC content and genome fragmentation levels exhibit interspecific variation, and chromosome breaking sites (CBSs) might be lost during evolution, resulting in the increase of multi-gene nanochromosome; (c) gene families associated with chitin metabolism and FoxO signaling pathway are expanded in E. aediculatus, suggesting their potential roles in environment adaptation and survival strategies of E. aediculatus; and (d) a programmed ribosomal frameshift (PRF) with a conservative motif 5′-AAATAR-3′ tends to occur in longer genes with more exons, and PRF genes play an important role in many cellular regulation processes. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s42995-023-00175-0. |
format | Online Article Text |
id | pubmed-10449743 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Springer Nature Singapore |
record_format | MEDLINE/PubMed |
spelling | pubmed-104497432023-08-26 Comparative genome analysis of three euplotid protists provides insights into the evolution of nanochromosomes in unicellular eukaryotic organisms Jin, Didi Li, Chao Chen, Xiao Byerly, Adam Stover, Naomi A. Zhang, Tengteng Shao, Chen Wang, Yurui Mar Life Sci Technol Research Paper One of the most diverse clades of ciliated protozoa, the class Spirotrichea, displays a series of unique characters in terms of eukaryotic macronuclear (MAC) genome, including high fragmentation that produces nanochromosomes. However, the genomic diversity and evolution of nanochromosomes and gene families for spirotrich MAC genomes are poorly understood. In this study, we assemble the MAC genome of a representative euplotid (a new model organism in Spirotrichea) species, Euplotes aediculatus. Our results indicate that: (a) the MAC genome includes 35,465 contigs with a total length of 97.3 Mb and a contig N50 of 3.4 kb, and contains 13,145 complete nanochromosomes and 43,194 predicted genes, with the majority of these nanochromosomes containing tiny introns and harboring only one gene; (b) genomic comparisons between E. aediculatus and other reported spirotrichs indicate that average GC content and genome fragmentation levels exhibit interspecific variation, and chromosome breaking sites (CBSs) might be lost during evolution, resulting in the increase of multi-gene nanochromosome; (c) gene families associated with chitin metabolism and FoxO signaling pathway are expanded in E. aediculatus, suggesting their potential roles in environment adaptation and survival strategies of E. aediculatus; and (d) a programmed ribosomal frameshift (PRF) with a conservative motif 5′-AAATAR-3′ tends to occur in longer genes with more exons, and PRF genes play an important role in many cellular regulation processes. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s42995-023-00175-0. Springer Nature Singapore 2023-05-28 /pmc/articles/PMC10449743/ /pubmed/37637252 http://dx.doi.org/10.1007/s42995-023-00175-0 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/ Open AccessThis 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 | Research Paper Jin, Didi Li, Chao Chen, Xiao Byerly, Adam Stover, Naomi A. Zhang, Tengteng Shao, Chen Wang, Yurui Comparative genome analysis of three euplotid protists provides insights into the evolution of nanochromosomes in unicellular eukaryotic organisms |
title | Comparative genome analysis of three euplotid protists provides insights into the evolution of nanochromosomes in unicellular eukaryotic organisms |
title_full | Comparative genome analysis of three euplotid protists provides insights into the evolution of nanochromosomes in unicellular eukaryotic organisms |
title_fullStr | Comparative genome analysis of three euplotid protists provides insights into the evolution of nanochromosomes in unicellular eukaryotic organisms |
title_full_unstemmed | Comparative genome analysis of three euplotid protists provides insights into the evolution of nanochromosomes in unicellular eukaryotic organisms |
title_short | Comparative genome analysis of three euplotid protists provides insights into the evolution of nanochromosomes in unicellular eukaryotic organisms |
title_sort | comparative genome analysis of three euplotid protists provides insights into the evolution of nanochromosomes in unicellular eukaryotic organisms |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10449743/ https://www.ncbi.nlm.nih.gov/pubmed/37637252 http://dx.doi.org/10.1007/s42995-023-00175-0 |
work_keys_str_mv | AT jindidi comparativegenomeanalysisofthreeeuplotidprotistsprovidesinsightsintotheevolutionofnanochromosomesinunicellulareukaryoticorganisms AT lichao comparativegenomeanalysisofthreeeuplotidprotistsprovidesinsightsintotheevolutionofnanochromosomesinunicellulareukaryoticorganisms AT chenxiao comparativegenomeanalysisofthreeeuplotidprotistsprovidesinsightsintotheevolutionofnanochromosomesinunicellulareukaryoticorganisms AT byerlyadam comparativegenomeanalysisofthreeeuplotidprotistsprovidesinsightsintotheevolutionofnanochromosomesinunicellulareukaryoticorganisms AT stovernaomia comparativegenomeanalysisofthreeeuplotidprotistsprovidesinsightsintotheevolutionofnanochromosomesinunicellulareukaryoticorganisms AT zhangtengteng comparativegenomeanalysisofthreeeuplotidprotistsprovidesinsightsintotheevolutionofnanochromosomesinunicellulareukaryoticorganisms AT shaochen comparativegenomeanalysisofthreeeuplotidprotistsprovidesinsightsintotheevolutionofnanochromosomesinunicellulareukaryoticorganisms AT wangyurui comparativegenomeanalysisofthreeeuplotidprotistsprovidesinsightsintotheevolutionofnanochromosomesinunicellulareukaryoticorganisms |