Literature DB >> 33552129

Mutational Dynamics of Aroid Chloroplast Genomes II.

Claudia L Henriquez1, Thomas B Croat2, Peter Poczai3, Ibrar Ahmed4.   

Abstract

The co-occurrence among single nucleotide polymorphisms (SNPs), insertions-deletions (InDels), and oligonucleotide repeats has been reported in prokaryote, eukaryote, and chloroplast genomes. Correlations among SNPs, InDels, and repeats have been investigated in the plant family Araceae previously using pair-wise sequence alignments of the chloroplast genomes of two morphotypes of one species, Colocasia esculenta belonging to subfamily Aroideae (crown group), and four species from the subfamily Lemnoideae, a basal group. The family Araceae is a large family comprising 3,645 species in 144 genera, grouped into eight subfamilies. In the current study, we performed 34 comparisons using 27 species from 7 subfamilies of Araceae to determine correlation coefficients among the mutational events at the family, subfamily, and genus levels. We express strength of the correlations as: negligible or very weak (0.10-0.19), weak (0.20-0.29), moderate (0.30-0.39), strong (0.40-0.69), very strong (0.70-0.99), and perfect (1.00). We observed strong/very strong correlations in most comparisons, whereas a few comparisons showed moderate correlations. The average correlation coefficient was recorded as 0.66 between "SNPs and InDels," 0.50 between "InDels and repeats," and 0.42 between "SNPs and repeats." In qualitative analyses, 95-100% of the repeats at family and sub-family level, while 36-86% of the repeats at genus level comparisons co-occurred with SNPs in the same bins. Our findings show that such correlations among mutational events exist throughout Araceae and support the hypothesis of distribution of oligonucleotide repeats as a proxy for mutational hotspots.
Copyright © 2021 Abdullah, Henriquez, Croat, Poczai and Ahmed.

Entities:  

Keywords:  Araceae (aroid); InDels (insertions/deletions); chloroplast genome; correlations; repeats

Year:  2021        PMID: 33552129      PMCID: PMC7854696          DOI: 10.3389/fgene.2020.610838

Source DB:  PubMed          Journal:  Front Genet        ISSN: 1664-8021            Impact factor:   4.599


  53 in total

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