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Structure, Activity, and Function of SETMAR Protein Lysine Methyltransferase

SETMAR is a protein lysine methyltransferase that is involved in several DNA processes, including DNA repair via the non-homologous end joining (NHEJ) pathway, regulation of gene expression, illegitimate DNA integration, and DNA decatenation. However, SETMAR is an atypical protein lysine methyltrans...

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Autor principal: Tellier, Michael
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8704517/
https://www.ncbi.nlm.nih.gov/pubmed/34947873
http://dx.doi.org/10.3390/life11121342
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author Tellier, Michael
author_facet Tellier, Michael
author_sort Tellier, Michael
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description SETMAR is a protein lysine methyltransferase that is involved in several DNA processes, including DNA repair via the non-homologous end joining (NHEJ) pathway, regulation of gene expression, illegitimate DNA integration, and DNA decatenation. However, SETMAR is an atypical protein lysine methyltransferase since in anthropoid primates, the SET domain is fused to an inactive DNA transposase. The presence of the DNA transposase domain confers to SETMAR a DNA binding activity towards the remnants of its transposable element, which has resulted in the emergence of a gene regulatory function. Both the SET and the DNA transposase domains are involved in the different cellular roles of SETMAR, indicating the presence of novel and specific functions in anthropoid primates. In addition, SETMAR is dysregulated in different types of cancer, indicating a potential pathological role. While some light has been shed on SETMAR functions, more research and new tools are needed to better understand the cellular activities of SETMAR and to investigate the therapeutic potential of SETMAR.
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spelling pubmed-87045172021-12-25 Structure, Activity, and Function of SETMAR Protein Lysine Methyltransferase Tellier, Michael Life (Basel) Review SETMAR is a protein lysine methyltransferase that is involved in several DNA processes, including DNA repair via the non-homologous end joining (NHEJ) pathway, regulation of gene expression, illegitimate DNA integration, and DNA decatenation. However, SETMAR is an atypical protein lysine methyltransferase since in anthropoid primates, the SET domain is fused to an inactive DNA transposase. The presence of the DNA transposase domain confers to SETMAR a DNA binding activity towards the remnants of its transposable element, which has resulted in the emergence of a gene regulatory function. Both the SET and the DNA transposase domains are involved in the different cellular roles of SETMAR, indicating the presence of novel and specific functions in anthropoid primates. In addition, SETMAR is dysregulated in different types of cancer, indicating a potential pathological role. While some light has been shed on SETMAR functions, more research and new tools are needed to better understand the cellular activities of SETMAR and to investigate the therapeutic potential of SETMAR. MDPI 2021-12-04 /pmc/articles/PMC8704517/ /pubmed/34947873 http://dx.doi.org/10.3390/life11121342 Text en © 2021 by the author. 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 Review
Tellier, Michael
Structure, Activity, and Function of SETMAR Protein Lysine Methyltransferase
title Structure, Activity, and Function of SETMAR Protein Lysine Methyltransferase
title_full Structure, Activity, and Function of SETMAR Protein Lysine Methyltransferase
title_fullStr Structure, Activity, and Function of SETMAR Protein Lysine Methyltransferase
title_full_unstemmed Structure, Activity, and Function of SETMAR Protein Lysine Methyltransferase
title_short Structure, Activity, and Function of SETMAR Protein Lysine Methyltransferase
title_sort structure, activity, and function of setmar protein lysine methyltransferase
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8704517/
https://www.ncbi.nlm.nih.gov/pubmed/34947873
http://dx.doi.org/10.3390/life11121342
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