高身材和脊柱侧凸与NPR3中一种新的纯合子功能缺失错义变异相关。

IF 1.7 4区 生物学 Q3 GENETICS & HEREDITY
Pierre Moffatt, Chantal Janelle, Valancy Miranda, Ghalib Bardai, Frank Rauch
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引用次数: 0

摘要

与npr3相关的高个子的特征是身材高大,大脚趾细长,手和足骨有额外的骨骺。这种情况是由影响利钠肽受体3 (NPR3)的双等位基因功能丧失变异引起的。据报道,来自四个不同家庭的五个人。在这里,我们描述了三个与npr3相关的高个子兄弟姐妹,他们身材高大(身高z分数在+2.9到+ 4.9之间),近端和中端指骨明显拉长。两个兄弟姐妹在指骨和掌骨上有额外的骨骺。所有三个兄弟姐妹都出现了脊柱侧凸,其中一人需要脊柱融合手术。腰椎骨密度相对较高。对一个兄弟姐妹的骨骼疾病基因面板进行测序,发现了NPR3的纯合错义变体(NM_001204375.2;c.382C > T;p.Pro128Ser)。Sanger测序显示在其他兄弟姐妹中也有相同的纯合变异。MC3T3-E1成骨前细胞的体外功能测试表明,携带p.p pro128ser变体的NPR3表达,但保留在内质网中,导致NPR3功能丧失。总之,NPR3中新的纯合子p.Pro128Ser功能缺失变异导致了与NPR3相关的高个子的典型特征,此外,还与脊柱侧凸相关。这些观察结果扩大了npr3相关高个子的基因型和表型谱。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Tall Stature and Scoliosis Associated With a Novel Homozygous Loss-of-Function Missense Variant in NPR3.

NPR3-related tall stature is characterized by tall stature, elongated big toes, and additional epiphyses in hand and foot bones. The condition is caused by biallelic loss-of-function variants affecting natriuretic peptide receptor 3 (NPR3). Five individuals from four different families have been reported. Here we describe three siblings with NPR3-related tall stature who were tall (height z-scores between +2.9 and + 4.9) and had markedly elongated proximal and middle phalanges. Two siblings had additional epiphyses in phalangeal and metacarpal bones. All three siblings developed scoliosis, requiring spinal fusion surgery in one individual. Lumbar spine bone mineral density appeared low considering the tall stature. Sequencing of a skeletal disorders gene panel in one sibling revealed a homozygous missense variant in NPR3 (NM_001204375.2; c.382C>T; p.Pro128Ser). Sanger sequencing demonstrated the same homozygous variant in the other siblings. In vitro functional testing in MC3T3-E1 preosteoblastic cells showed that NPR3 carrying the p.Pro128Ser variant was expressed but was retained in the endoplasmic reticulum, leading to loss of NPR3 function. In conclusion, the novel homozygous p.Pro128Ser loss-of-function variant in NPR3 led to the typical features of NPR3-related tall stature and, in addition, was associated with scoliosis. These observations expand the genotypic and phenotypic spectrum of NPR3-related tall stature.

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来源期刊
CiteScore
3.50
自引率
5.00%
发文量
432
审稿时长
2-4 weeks
期刊介绍: The American Journal of Medical Genetics - Part A (AJMG) gives you continuous coverage of all biological and medical aspects of genetic disorders and birth defects, as well as in-depth documentation of phenotype analysis within the current context of genotype/phenotype correlations. In addition to Part A , AJMG also publishes two other parts: Part B: Neuropsychiatric Genetics , covering experimental and clinical investigations of the genetic mechanisms underlying neurologic and psychiatric disorders. Part C: Seminars in Medical Genetics , guest-edited collections of thematic reviews of topical interest to the readership of AJMG .
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