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Identification and molecular analysis of RNF31 Q622H germline polymorphism

The linear ubiquitin chain assembly complex (LUBAC), which is composed of RING finger protein 31 (RNF31), RANBP2-type and C3HC4-type zinc finger containing 1 and SHANK-associated RH domain interactor subunits, is the only ubiquitin ligase to generate Met1-linked linear ubiquitin chains. Linear ubiqu...

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Autores principales: Nakazawa, Seshiru, Mamiya, Ryo, Kawabata-Iwakawa, Reika, Oikawa, Daisuke, Kaira, Kyoichi, Tokunaga, Fuminori, Nobusawa, Sumihito, Sato, Yusuke, Sasaki, Atsushi, Yajima, Toshiki, Shirabe, Ken
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9533369/
https://www.ncbi.nlm.nih.gov/pubmed/36276481
http://dx.doi.org/10.3892/ol.2022.13514
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author Nakazawa, Seshiru
Mamiya, Ryo
Kawabata-Iwakawa, Reika
Oikawa, Daisuke
Kaira, Kyoichi
Tokunaga, Fuminori
Nobusawa, Sumihito
Sato, Yusuke
Sasaki, Atsushi
Yajima, Toshiki
Shirabe, Ken
author_facet Nakazawa, Seshiru
Mamiya, Ryo
Kawabata-Iwakawa, Reika
Oikawa, Daisuke
Kaira, Kyoichi
Tokunaga, Fuminori
Nobusawa, Sumihito
Sato, Yusuke
Sasaki, Atsushi
Yajima, Toshiki
Shirabe, Ken
author_sort Nakazawa, Seshiru
collection PubMed
description The linear ubiquitin chain assembly complex (LUBAC), which is composed of RING finger protein 31 (RNF31), RANBP2-type and C3HC4-type zinc finger containing 1 and SHANK-associated RH domain interactor subunits, is the only ubiquitin ligase to generate Met1-linked linear ubiquitin chains. Linear ubiquitin chains regulate canonical NF-κB activation and cell death. Single nucleotide polymorphisms in RNF31, such as Q584H and Q622L, are known to cause the activated B cell-like subtype of diffuse large B cell lymphoma (ABC-DLBCL) because of enhanced LUBAC-mediated NF-κB activation. The present study identified a novel Q622H polymorphism of RNF31 in two patients with lung cancer, one of whom had concurrent ABC-DLBCL. Immunohistochemical analyses revealed that although the expression of RNF31 was elevated in both patients, only the ABC-DLBCL specimen showed increased NF-κB activation. Cancer panel analysis showed that the Q622H-related ABC-DLBCL did not harbor co-mutations that were previously reported in Q584H-/Q622L-related ABC-DLBCL. Furthermore, in contrast to Q584H and Q622L, Q622H showed no enhancement effects on LUBAC and NF-κB activity in vitro compared with wild-type RNF31. The present study's structural prediction suggested that the electrostatic interaction related to the Q622 residue may not have had an important role in LUBAC formation. In conclusion, the molecular mechanism and mutational background of RNF31 Q622H differed from that of RNF31 Q584H or Q622L. Furthermore, RNF31 Q622H appeared not to induce NF-κB activation in lung cancer.
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spelling pubmed-95333692022-10-20 Identification and molecular analysis of RNF31 Q622H germline polymorphism Nakazawa, Seshiru Mamiya, Ryo Kawabata-Iwakawa, Reika Oikawa, Daisuke Kaira, Kyoichi Tokunaga, Fuminori Nobusawa, Sumihito Sato, Yusuke Sasaki, Atsushi Yajima, Toshiki Shirabe, Ken Oncol Lett Articles The linear ubiquitin chain assembly complex (LUBAC), which is composed of RING finger protein 31 (RNF31), RANBP2-type and C3HC4-type zinc finger containing 1 and SHANK-associated RH domain interactor subunits, is the only ubiquitin ligase to generate Met1-linked linear ubiquitin chains. Linear ubiquitin chains regulate canonical NF-κB activation and cell death. Single nucleotide polymorphisms in RNF31, such as Q584H and Q622L, are known to cause the activated B cell-like subtype of diffuse large B cell lymphoma (ABC-DLBCL) because of enhanced LUBAC-mediated NF-κB activation. The present study identified a novel Q622H polymorphism of RNF31 in two patients with lung cancer, one of whom had concurrent ABC-DLBCL. Immunohistochemical analyses revealed that although the expression of RNF31 was elevated in both patients, only the ABC-DLBCL specimen showed increased NF-κB activation. Cancer panel analysis showed that the Q622H-related ABC-DLBCL did not harbor co-mutations that were previously reported in Q584H-/Q622L-related ABC-DLBCL. Furthermore, in contrast to Q584H and Q622L, Q622H showed no enhancement effects on LUBAC and NF-κB activity in vitro compared with wild-type RNF31. The present study's structural prediction suggested that the electrostatic interaction related to the Q622 residue may not have had an important role in LUBAC formation. In conclusion, the molecular mechanism and mutational background of RNF31 Q622H differed from that of RNF31 Q584H or Q622L. Furthermore, RNF31 Q622H appeared not to induce NF-κB activation in lung cancer. D.A. Spandidos 2022-09-21 /pmc/articles/PMC9533369/ /pubmed/36276481 http://dx.doi.org/10.3892/ol.2022.13514 Text en Copyright: © Nakazawa et al. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made.
spellingShingle Articles
Nakazawa, Seshiru
Mamiya, Ryo
Kawabata-Iwakawa, Reika
Oikawa, Daisuke
Kaira, Kyoichi
Tokunaga, Fuminori
Nobusawa, Sumihito
Sato, Yusuke
Sasaki, Atsushi
Yajima, Toshiki
Shirabe, Ken
Identification and molecular analysis of RNF31 Q622H germline polymorphism
title Identification and molecular analysis of RNF31 Q622H germline polymorphism
title_full Identification and molecular analysis of RNF31 Q622H germline polymorphism
title_fullStr Identification and molecular analysis of RNF31 Q622H germline polymorphism
title_full_unstemmed Identification and molecular analysis of RNF31 Q622H germline polymorphism
title_short Identification and molecular analysis of RNF31 Q622H germline polymorphism
title_sort identification and molecular analysis of rnf31 q622h germline polymorphism
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9533369/
https://www.ncbi.nlm.nih.gov/pubmed/36276481
http://dx.doi.org/10.3892/ol.2022.13514
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