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Microbial Type IA Topoisomerase C-Terminal Domain Sequence Motifs, Distribution and Combination

Type IA topoisomerases have highly conserved catalytic N-terminal domains for the cleaving and rejoining of a single DNA/RNA strand that have been extensively characterized. In contrast, the C-terminal region has been less covered. Two major types of small tandem C-terminal domains, Topo_C_ZnRpt (co...

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Autores principales: Diaz, Brenda, Mederos, Christopher, Tan, Kemin, Tse-Dinh, Yuk-Ching
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9369019/
https://www.ncbi.nlm.nih.gov/pubmed/35955842
http://dx.doi.org/10.3390/ijms23158709
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author Diaz, Brenda
Mederos, Christopher
Tan, Kemin
Tse-Dinh, Yuk-Ching
author_facet Diaz, Brenda
Mederos, Christopher
Tan, Kemin
Tse-Dinh, Yuk-Ching
author_sort Diaz, Brenda
collection PubMed
description Type IA topoisomerases have highly conserved catalytic N-terminal domains for the cleaving and rejoining of a single DNA/RNA strand that have been extensively characterized. In contrast, the C-terminal region has been less covered. Two major types of small tandem C-terminal domains, Topo_C_ZnRpt (containing C4 zinc finger) and Topo_C_Rpt (without cysteines) were initially identified in Escherichia coli and Mycobacterium tuberculosis topoisomerase I, respectively. Their structures and interaction with DNA oligonucleotides have been revealed in structural studies. Here, we first present the diverse distribution and combinations of these two structural elements in various bacterial topoisomerase I (TopA). Previously, zinc fingers have not been seen in type IA topoisomerases from well-studied fungal species within the phylum Ascomycota. In our extended studies of C-terminal DNA-binding domains, the presence of zf-GRF and zf-CCHC types of zinc fingers in topoisomerase III (Top3) from fungi species in many phyla other than Ascomycota has drawn our attention. We secondly analyze the distribution and combination of these fungal zf-GRF- and zf-CCHC-containing domains. Their potential structures and DNA-binding mechanism are evaluated. The highly diverse arrangements and combinations of these DNA/RNA-binding domains in microbial type IA topoisomerase C-terminal regions have important implications for their interactions with nucleic acids and protein partners as part of their physiological functions.
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spelling pubmed-93690192022-08-12 Microbial Type IA Topoisomerase C-Terminal Domain Sequence Motifs, Distribution and Combination Diaz, Brenda Mederos, Christopher Tan, Kemin Tse-Dinh, Yuk-Ching Int J Mol Sci Article Type IA topoisomerases have highly conserved catalytic N-terminal domains for the cleaving and rejoining of a single DNA/RNA strand that have been extensively characterized. In contrast, the C-terminal region has been less covered. Two major types of small tandem C-terminal domains, Topo_C_ZnRpt (containing C4 zinc finger) and Topo_C_Rpt (without cysteines) were initially identified in Escherichia coli and Mycobacterium tuberculosis topoisomerase I, respectively. Their structures and interaction with DNA oligonucleotides have been revealed in structural studies. Here, we first present the diverse distribution and combinations of these two structural elements in various bacterial topoisomerase I (TopA). Previously, zinc fingers have not been seen in type IA topoisomerases from well-studied fungal species within the phylum Ascomycota. In our extended studies of C-terminal DNA-binding domains, the presence of zf-GRF and zf-CCHC types of zinc fingers in topoisomerase III (Top3) from fungi species in many phyla other than Ascomycota has drawn our attention. We secondly analyze the distribution and combination of these fungal zf-GRF- and zf-CCHC-containing domains. Their potential structures and DNA-binding mechanism are evaluated. The highly diverse arrangements and combinations of these DNA/RNA-binding domains in microbial type IA topoisomerase C-terminal regions have important implications for their interactions with nucleic acids and protein partners as part of their physiological functions. MDPI 2022-08-05 /pmc/articles/PMC9369019/ /pubmed/35955842 http://dx.doi.org/10.3390/ijms23158709 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Diaz, Brenda
Mederos, Christopher
Tan, Kemin
Tse-Dinh, Yuk-Ching
Microbial Type IA Topoisomerase C-Terminal Domain Sequence Motifs, Distribution and Combination
title Microbial Type IA Topoisomerase C-Terminal Domain Sequence Motifs, Distribution and Combination
title_full Microbial Type IA Topoisomerase C-Terminal Domain Sequence Motifs, Distribution and Combination
title_fullStr Microbial Type IA Topoisomerase C-Terminal Domain Sequence Motifs, Distribution and Combination
title_full_unstemmed Microbial Type IA Topoisomerase C-Terminal Domain Sequence Motifs, Distribution and Combination
title_short Microbial Type IA Topoisomerase C-Terminal Domain Sequence Motifs, Distribution and Combination
title_sort microbial type ia topoisomerase c-terminal domain sequence motifs, distribution and combination
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9369019/
https://www.ncbi.nlm.nih.gov/pubmed/35955842
http://dx.doi.org/10.3390/ijms23158709
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AT tankemin microbialtypeiatopoisomerasecterminaldomainsequencemotifsdistributionandcombination
AT tsedinhyukching microbialtypeiatopoisomerasecterminaldomainsequencemotifsdistributionandcombination