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Comparative Plastome Genomics, Taxonomic Delimitation and Evolutionary Divergences of Tetraena Hamiensis Var. Qatarensis and Tetraena Simplex (Zygophyllaceae)

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Journal Sci Rep
Specialty Science
Date 2023 May 8
PMID 37156827
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Abstract

The Zygophyllum and Tetraena genera are intriguingly important ecologically and medicinally. Based on morphological characteristics, T. hamiensis var. qatarensis, and T. simplex were transferred from Zygophyllum to Tetraena with the least genomic datasets available. Hence, we sequenced the T. hamiensis and T. simplex and performed in-depth comparative genomics, phylogenetic analysis, and estimated time divergences. The complete plastomes ranged between 106,720 and 106,446 bp-typically smaller than angiosperms plastomes. The plastome circular genomes are divided into large single-copy regions (~ 80,964 bp), small single-copy regions (~ 17,416 bp), and two inverted repeats regions (~ 4170 bp) in both Tetraena species. An unusual shrinkage of IR regions 16-24 kb was identified. This resulted in the loss of 16 genes, including 11 ndh genes which encode the NADH dehydrogenase subunits, and a significant size reduction of Tetraena plastomes compared to other angiosperms. The inter-species variations and similarities were identified using genome-wide comparisons. Phylogenetic trees generated by analyzing the whole plastomes, protein-coding genes, matK, rbcL, and cssA genes exhibited identical topologies, indicating that both species are sisters to the genus Tetraena and may not belong to Zygophyllum. Similarly, based on the entire plastome and proteins coding genes datasets, the time divergence of Zygophyllum and Tetraena was 36.6 Ma and 34.4 Ma, respectively. Tetraena stem ages were 31.7 and 18.2 Ma based on full plastome and protein-coding genes. The current study presents the plastome as a distinguishing and identification feature among the closely related Tetraena and Zygophyllum species. It can be potentially used as a universal super-barcode for identifying plants.

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References
1.
Shapiro J, von Sternberg R . Why repetitive DNA is essential to genome function. Biol Rev Camb Philos Soc. 2005; 80(2):227-50. DOI: 10.1017/s1464793104006657. View

2.
Abdullah , Henriquez C, Croat T, Poczai P, Ahmed I . Mutational Dynamics of Aroid Chloroplast Genomes II. Front Genet. 2021; 11:610838. PMC: 7854696. DOI: 10.3389/fgene.2020.610838. View

3.
Khan A, Asaf S, Khan A, Khan A, Al-Harrasi A, Al-Sudairy O . Complete chloroplast genomes of medicinally important species and comparative analyses with related species from Lamiaceae. PeerJ. 2019; 7:e7260. PMC: 6625504. DOI: 10.7717/peerj.7260. View

4.
Frazer K, Pachter L, Poliakov A, Rubin E, Dubchak I . VISTA: computational tools for comparative genomics. Nucleic Acids Res. 2004; 32(Web Server issue):W273-9. PMC: 441596. DOI: 10.1093/nar/gkh458. View

5.
Perry A, Wolfe K . Nucleotide substitution rates in legume chloroplast DNA depend on the presence of the inverted repeat. J Mol Evol. 2002; 55(5):501-8. DOI: 10.1007/s00239-002-2333-y. View