Literature DB >> 18262818

Identification of a novel mutation V2321M of the cardiac ryanodine receptor gene of sudden unexplained death and a phenotypic study of the gene mutations.

Hajime Nishio1, Misa Iwata, Akiyoshi Tamura, Tokiko Miyazaki, Kento Tsuboi, Koichi Suzuki.   

Abstract

Mutations of the cardiac ryanodine receptor (RyR2) gene cause catecholaminergic polymorphic ventricular tachycardia, which sometimes results in a finding of sudden unexplained death (SUD) at autopsy. We found a novel mutation (V2321M) in exon 46 of the RyR2 gene in a SUD case. V2321M was localized in a highly conservative site of the RyR2 gene, but was not found in 400 reference alleles. We previously reported two SUD cases with R420W mutations in exon 14 of the RyR2 gene. We examined possible phenotypic characteristics of all three of these cases of SUD with the RyR2 gene mutations. All cases displayed mesenteric lymph node hypertrophy as well as tendencies for aortic narrowing. By contrast, only one of the 14 SUD cases without RyR2 mutations displayed these phenotypes. This study supports the concept that postmortem genetic testing of RyR2 mutations should be considered in autopsy examinations of SUD cases. It also raises the possibility that some cases with RyR2 mutations may display phenotypic changes in lymphoid and cardiovascular organs.

Entities:  

Mesh:

Substances:

Year:  2008        PMID: 18262818     DOI: 10.1016/j.legalmed.2007.12.003

Source DB:  PubMed          Journal:  Leg Med (Tokyo)        ISSN: 1344-6223            Impact factor:   1.376


  3 in total

1.  Cytosolic Ca2+-dependent Ca2+ release activity primarily determines the ER Ca2+ level in cells expressing the CPVT-linked mutant RYR2.

Authors:  Nagomi Kurebayashi; Takashi Murayama; Ryosaku Ota; Fumiyoshi Yamashita; Junji Suzuki; Kazunori Kanemaru; Takuya Kobayashi; Seiko Ohno; Minoru Horie; Masamitsu Iino; Takashi Sakurai
Journal:  J Gen Physiol       Date:  2022-04-21       Impact factor: 4.000

2.  The RYR2-encoded ryanodine receptor/calcium release channel in patients diagnosed previously with either catecholaminergic polymorphic ventricular tachycardia or genotype negative, exercise-induced long QT syndrome: a comprehensive open reading frame mutational analysis.

Authors:  Argelia Medeiros-Domingo; Zahurul A Bhuiyan; David J Tester; Nynke Hofman; Hennie Bikker; J Peter van Tintelen; Marcel M A M Mannens; Arthur A M Wilde; Michael J Ackerman
Journal:  J Am Coll Cardiol       Date:  2009-11-24       Impact factor: 24.094

3.  Identification of an ethnic-specific variant (V207M) of the KCNQ1 cardiac potassium channel gene in sudden unexplained death and implications from a knock-in mouse model.

Authors:  Hajime Nishio; Masayoshi Kuwahara; Hirokazu Tsubone; Yoshiro Koda; Takako Sato; Shinya Fukunishi; Akiyoshi Tamura; Koichi Suzuki
Journal:  Int J Legal Med       Date:  2009-02-07       Impact factor: 2.686

  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.