Genome Expansion by tRNA +1 Frameshifting at Quadruplet Codons

2022 ◽  
pp. 167440
Author(s):  
Howard Gamper ◽  
Isao Masuda ◽  
Ya-Ming Hou
Keyword(s):  
2013 ◽  
Vol 9 (7) ◽  
pp. e1003500 ◽  
Author(s):  
Chris Lauber ◽  
Jelle J. Goeman ◽  
Maria del Carmen Parquet ◽  
Phan Thi Nga ◽  
Eric J. Snijder ◽  
...  

2019 ◽  
Vol 12 (1) ◽  
Author(s):  
Stephen J. Mondo ◽  
Diego Javier Jiménez ◽  
Ronald E. Hector ◽  
Anna Lipzen ◽  
Mi Yan ◽  
...  

Abstract Background Particular species of the genus Coniochaeta (Sordariomycetes) exhibit great potential for bioabatement of furanic compounds and have been identified as an underexplored source of novel lignocellulolytic enzymes, especially Coniochaeta ligniaria. However, there is a lack of information about their genomic features and metabolic capabilities. Here, we report the first in-depth genome/transcriptome survey of a Coniochaeta species (strain 2T2.1). Results The genome of Coniochaeta sp. strain 2T2.1 has a size of 74.53 Mbp and contains 24,735 protein-encoding genes. Interestingly, we detected a genome expansion event, resulting ~ 98% of the assembly being duplicated with 91.9% average nucleotide identity between the duplicated regions. The lack of gene loss, as well as the high divergence and strong genome-wide signatures of purifying selection between copies indicates that this is likely a recent duplication, which arose through hybridization between two related Coniochaeta-like species (allopolyploidization). Phylogenomic analysis revealed that 2T2.1 is related Coniochaeta sp. PMI546 and Lecythophora sp. AK0013, which both occur endophytically. Based on carbohydrate-active enzyme (CAZy) annotation, we observed that even after in silico removal of its duplicated content, the 2T2.1 genome contains exceptional lignocellulolytic machinery. Moreover, transcriptomic data reveal the overexpression of proteins affiliated to CAZy families GH11, GH10 (endoxylanases), CE5, CE1 (xylan esterases), GH62, GH51 (α-l-arabinofuranosidases), GH12, GH7 (cellulases), and AA9 (lytic polysaccharide monoxygenases) when the fungus was grown on wheat straw compared with glucose as the sole carbon source. Conclusions We provide data that suggest that a recent hybridization between the genomes of related species may have given rise to Coniochaeta sp. 2T2.1. Moreover, our results reveal that the degradation of arabinoxylan, xyloglucan and cellulose are key metabolic processes in strain 2T2.1 growing on wheat straw. Different genes for key lignocellulolytic enzymes were identified, which can be starting points for production, characterization and/or supplementation of enzyme cocktails used in saccharification of agricultural residues. Our findings represent first steps that enable a better understanding of the reticulate evolution and “eco-enzymology” of lignocellulolytic Coniochaeta species.


2006 ◽  
Vol 16 (20) ◽  
pp. R872-R873 ◽  
Author(s):  
Mark C. Ungerer ◽  
Suzanne C. Strakosh ◽  
Ying Zhen

2018 ◽  
Vol 10 (6) ◽  
pp. 1526-1532 ◽  
Author(s):  
Yi-Ming Tsai ◽  
An Chang ◽  
Chih-Horng Kuo
Keyword(s):  

2020 ◽  
Vol 117 (32) ◽  
pp. 19359-19366
Author(s):  
Wanding Zhou ◽  
Gangning Liang ◽  
Peter L. Molloy ◽  
Peter A. Jones

Multicellular eukaryotic genomes show enormous differences in size. A substantial part of this variation is due to the presence of transposable elements (TEs). They contribute significantly to a cell’s mass of DNA and have the potential to become involved in host gene control. We argue that the suppression of their activities by methylation of the C–phosphate–G (CpG) dinucleotide in DNA is essential for their long-term accommodation in the host genome and, therefore, to its expansion. An inevitable consequence of cytosine methylation is an increase in C-to-T transition mutations via deamination, which causes CpG loss. Cytosine deamination is often needed for TEs to take on regulatory functions in the host genome. Our study of the whole-genome sequences of 53 organisms showed a positive correlation between the size of a genome and the percentage of TEs it contains, as well as a negative correlation between size and the CpG observed/expected (O/E) ratio in both TEs and the host DNA. TEs are seldom found at promoters and transcription start sites, but they are found more at enhancers, particularly after they have accumulated C-to-T and other mutations. Therefore, the methylation of TE DNA allows for genome expansion and also leads to new opportunities for gene control by TE-based regulatory sites.


PLoS ONE ◽  
2019 ◽  
Vol 14 (6) ◽  
pp. e0218204 ◽  
Author(s):  
Harshita Yakkala ◽  
Devyani Samantarrai ◽  
Michael Gribskov ◽  
Dayananda Siddavattam

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