Weber, Stefanie, Ramirez, Christina M. and Doerfler, Walter ORCID: 0000-0002-9971-0138 (2022). Ubiquitous Micro-Modular Homologies among Genomes from Viruses to Bacteria to Human Mitochondrial DNA: Platforms for Recombination during Evolution? Viruses-Basel, 14 (5). BASEL: MDPI. ISSN 1999-4915

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Abstract

The emerging Severe Acute Respiratory Syndrome Coronavirus-2 (SARS-CoV-2) and its variants have raised tantalizing questions about evolutionary mechanisms that continue to shape biology today. We have compared the nucleotide sequence of SARS-CoV-2 RNA to that of genomes of many different viruses, of endosymbiotic proteobacterial and bacterial DNAs, and of human mitochondrial DNA. The entire 4,641,652 nt DNA sequence of Escherichia coli K12 has been computer-matched to SARS-CoV-2 RNA. Numerous, very similar micro-modular clusters of 3 to 13 nucleotides lengths were detected with sequence identities of 40 to >50% in specific genome segments between SARS-CoV-2 and the investigated genomes. These clusters were part of patch-type homologies. Control sequence comparisons between 1000 randomly computer-composed sequences of 29.9 kb and with the A, C, G, T base composition of SARS-CoV-2 genome versus the reference Wuhan SARS-CoV-2 sequence showed similar patterns of sequence homologies. The universal A, C, G, T genetic coding mode might have succeeded in evolution due in part to its built-in capacity to select for a substantial reservoir of micro-modular domains and employ them as platforms for integrative recombination. Their role in SARS-CoV-2 interspecies transition and the generation of variants appears likely, but their actual involvement will require detailed investigations.

Item Type: Journal Article
Creators:
CreatorsEmailORCIDORCID Put Code
Weber, StefanieUNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Ramirez, Christina M.UNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Doerfler, WalterUNSPECIFIEDorcid.org/0000-0002-9971-0138UNSPECIFIED
URN: urn:nbn:de:hbz:38-677141
DOI: 10.3390/v14050885
Journal or Publication Title: Viruses-Basel
Volume: 14
Number: 5
Date: 2022
Publisher: MDPI
Place of Publication: BASEL
ISSN: 1999-4915
Language: English
Faculty: Unspecified
Divisions: Unspecified
Subjects: no entry
Uncontrolled Keywords:
KeywordsLanguage
ADENOVIRUS-TYPE-12 DNA; INTEGRATION SITES; HAMSTER; SEQUENCE; EXCISION; CELLSMultiple languages
VirologyMultiple languages
URI: http://kups.ub.uni-koeln.de/id/eprint/67714

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