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Tissue-selective alternate promoters guide NLRP6 expression

Nathan A Bracey, Jaye M Platnich, Arthur Lau, Hyunjae Chung, View ORCID ProfileM Eric Hyndman, View ORCID ProfileJustin A MacDonald, View ORCID ProfileJustin Chun, Paul L Beck, Stephen E Girardin, Paul MK Gordon, View ORCID ProfileDaniel A Muruve  Correspondence email
Nathan A Bracey
1Department of Medicine, University of Calgary, Calgary, Canada
2Snyder Institute for Chronic Disease, University of Calgary, Calgary, Canada
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Jaye M Platnich
3Department of Medicine, University of Alberta, Edmonton, Canada
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Arthur Lau
1Department of Medicine, University of Calgary, Calgary, Canada
2Snyder Institute for Chronic Disease, University of Calgary, Calgary, Canada
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Hyunjae Chung
1Department of Medicine, University of Calgary, Calgary, Canada
2Snyder Institute for Chronic Disease, University of Calgary, Calgary, Canada
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M Eric Hyndman
4Department of Surgery, University of Calgary, Calgary, Canada
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  • ORCID record for M Eric Hyndman
Justin A MacDonald
5Department of Biochemistry and Molecular Biology, University of Calgary, Calgary, Canada
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  • ORCID record for Justin A MacDonald
Justin Chun
1Department of Medicine, University of Calgary, Calgary, Canada
2Snyder Institute for Chronic Disease, University of Calgary, Calgary, Canada
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  • ORCID record for Justin Chun
Paul L Beck
1Department of Medicine, University of Calgary, Calgary, Canada
2Snyder Institute for Chronic Disease, University of Calgary, Calgary, Canada
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Stephen E Girardin
6Department of Laboratory Medicine and Pathobiology, University of Toronto, Toronto, Canada
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Paul MK Gordon
7Centre for Health Genomics and Informatics, University of Calgary, Calgary, Canada
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Daniel A Muruve
1Department of Medicine, University of Calgary, Calgary, Canada
2Snyder Institute for Chronic Disease, University of Calgary, Calgary, Canada
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  • ORCID record for Daniel A Muruve
  • For correspondence: dmuruve@ucalgary.ca
Published 29 December 2020. DOI: 10.26508/lsa.202000897
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Abstract

The pryin domain (PYD) domain is involved in protein interactions that lead to assembly of immune-sensing complexes such as inflammasomes. The repertoire of PYD-containing genes expressed by a cell type arms tissues with responses against a range of stimuli. The transcriptional regulation of the PYD gene family however is incompletely understood. Alternative promoter utilization was identified as a mechanism regulating the tissue distribution of human PYD gene family members, including NLRP6 that is translationally silenced outside of intestinal tissue. Results show that alternative transcriptional promoters mediate NLRP6 silencing in mice and humans, despite no upstream genomic synteny. Human NLRP6 contains an internal alternative promoter within exon 2 of the PYD, resulting in a truncated mRNA in nonintestinal tissue. In mice, a proximal promoter was used that expanded the 5′ leader sequence restricting nuclear export and abolishing translational efficiency. Nlrp6 was dispensable in disease models targeting the kidney, which expresses noncanonical isoforms. Thus, alternative promoter use is a critical mechanism not just for isoform modulation but for determining expression profile and function of PYD family members.

  • Received August 28, 2020.
  • Revision received December 12, 2020.
  • Accepted December 15, 2020.
  • © 2020 Bracey et al.
Creative Commons logoCreative Commons logohttps://creativecommons.org/licenses/by/4.0/

This article is available under a Creative Commons License (Attribution 4.0 International, as described at https://creativecommons.org/licenses/by/4.0/).

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Alternate promoters regulate NLRP6
Nathan A Bracey, Jaye M Platnich, Arthur Lau, Hyunjae Chung, M Eric Hyndman, Justin A MacDonald, Justin Chun, Paul L Beck, Stephen E Girardin, Paul MK Gordon, Daniel A Muruve
Life Science Alliance Dec 2020, 4 (3) e202000897; DOI: 10.26508/lsa.202000897

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Alternate promoters regulate NLRP6
Nathan A Bracey, Jaye M Platnich, Arthur Lau, Hyunjae Chung, M Eric Hyndman, Justin A MacDonald, Justin Chun, Paul L Beck, Stephen E Girardin, Paul MK Gordon, Daniel A Muruve
Life Science Alliance Dec 2020, 4 (3) e202000897; DOI: 10.26508/lsa.202000897
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Volume 4, No. 3
March 2021
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