A Novel Mutation in NKX2-1 Shows Dominant-Negative Effects only in the Presence of PAX8

Hiroyuki Shinohara, Masaki Takagi, Kimiko Ito, Eri Shimizu, Ryuji Fukuzawa, Tomonobu Hasegawa

研究成果: Article査読

5 被引用数 (Scopus)

抄録

To date, >100 mutations in NKX2-1 have been described. Most NKX2-1 mutations are assumed to result in brain-lung-thyroid syndrome through haploinsufficiency, and only five NKX2-1 mutations with dominant-negative effects have been reported so far. In this case report, an additional patient with brain-lung-thyroid syndrome is reported, carrying a novel heterozygous mutation, c.533G>C (p.R178P), in the homeobox of NKX2-1. This mutation has been proven to be a dominant-negative mutation by an in vitro functional assay. Of note, the dominant-negative effect of R178P-NKX2-1 was shown only in the presence of PAX8.

本文言語English
ページ(範囲)1071-1073
ページ数3
ジャーナルThyroid
28
8
DOI
出版ステータスPublished - 2018 8

ASJC Scopus subject areas

  • 内分泌学、糖尿病および代謝内科学
  • 内分泌学

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