一种新的同卵性致病性LEPR变体,在塞内加尔儿童中引起严重的早期肥胖
Virginie Deswarte1, Louis Lebreton1, Pascal Barat2
1Department of Biochemistry, Bordeaux University Hospital, Bordeaux, France.
Obesity research & clinical practice
|May 7, 2025
概括
莱普受体 (LEPR) 基因的新型遗传突变导致幼儿早期出现严重的肥胖和超. 这一发现强调了对单一性肥胖的基因测试和个性化治疗策略的重要性.
科学领域:
- 遗传学 遗传学 是一个
- 儿科 儿科 儿科
- 内分泌学 在内分泌学.
背景情况:
- 早期出现的肥胖症是一个严重的健康问题,具有复杂的病因.
- 单一的肥胖形式虽然很少见,但在严重的早期发病病例中起着至关重要的作用.
- 影响食欲调节的遗传因素在儿科体重管理中至关重要.
研究的目的:
- 调查塞内加尔儿童早期严重肥胖和多食症的遗传基础.
- 识别与儿童肥胖相关的新型遗传变异.
- 了解已识别的基因突变对勒普丁受体信号传递的功能后果.
主要方法:
- 一个三岁儿童的病例研究,患有严重的肥胖和过.
- 用于遗传分析的全外体序列测序.
- 功能性测试,以评估鉴定出的突变对莱普受体功能的影响.
主要成果:
- 在LEPR基因中发现了一种新型同卵性变异 (c.3190 G>T; p.(Glu1064Ter)).
- 这种突变导致了截断的变化,导致瘦素受体信号受损.
- 这个孩子从出生开始就出现了严重的肥胖和高,这与勒素通路功能障碍相一致.
结论:
- 这一案例突出了由于LEPR突变导致的早期肥胖的新奇单一原因.
- 对这些变异的基因鉴定对于有针对性的治疗干预至关重要.
- 了解瘦素受体信号缺陷可以指导儿童肥胖的临床管理.
相关概念视频
Lethal Alleles
15.4K
Agouti: A Lethal Allele
Lucien Cuénot discovered lethal alleles in 1905 while studying the inheritance of coat color in mice. The agouti gene is responsible for the color of the coat in mice. This gene codes for an agouti-signaling protein, which is responsible for melanin distribution in mammals. The wild-type allele gives rise to gray-brown coat color in mice, while the mutant allele gives rise to yellow coat color. In addition to coat color, the agouti gene is associated with the yellow...
Lucien Cuénot discovered lethal alleles in 1905 while studying the inheritance of coat color in mice. The agouti gene is responsible for the color of the coat in mice. This gene codes for an agouti-signaling protein, which is responsible for melanin distribution in mammals. The wild-type allele gives rise to gray-brown coat color in mice, while the mutant allele gives rise to yellow coat color. In addition to coat color, the agouti gene is associated with the yellow...
15.4K
Cystic Fibrosis: Pathogenesis
199
Cystic fibrosis (CF), an autosomal recessive disorder, significantly affects the function of exocrine glands. This genetically inherited disease is characterized by the production of thick and sticky mucus, which can severely affect various organs and systems in the body.
CF is primarily caused by a genetic mutation in a chromosome 7 gene coding for the cystic fibrosis transmembrane conductance regulator (CFTR) protein. The most common gene mutation leading to CF is the ΔF508 mutation,...
CF is primarily caused by a genetic mutation in a chromosome 7 gene coding for the cystic fibrosis transmembrane conductance regulator (CFTR) protein. The most common gene mutation leading to CF is the ΔF508 mutation,...
199
Pleiotropy
40.3K
Pleiotropy is the phenomenon in which a single gene impacts multiple, seemingly unrelated phenotypic traits. For example, defects in the SOX10 gene cause Waardenburg Syndrome Type 4, or WS4, which can cause defects in pigmentation, hearing impairments, and an absence of intestinal contractions necessary for elimination. This diversity of phenotypes results from the expression pattern of SOX10 in early embryonic and fetal development. SOX10 is found in neural crest cells that form melanocytes,...
40.3K
Genetic Lingo
102.3K
Overview
102.3K
Incomplete Dominance
22.2K
Gregor Mendel's work (1822 - 1884) was primarily focused on pea plants. Through his initial experiments, he determined that every gene in a diploid cell has two variants called alleles inherited from each parent. He suggested that amongst these two alleles, one allele is dominant in character and the other recessive. The combination of alleles determines the phenotype of a gene in an organism.
22.2K
Lysosomal Hydrolases
3.8K
Lysosomes are the site for the degradation of macromolecules and biological polymers released during membrane trafficking events such as secretory, endocytic, autophagic, and phagocytic pathways. The membrane-enclosed area of the lysosome, called the lumen, contains hydrolytic enzymes active in an acidic environment. These acid hydrolases are functional at a pH between 4.5 and 5 and are involved in cellular processes such as cell signaling, energy metabolism, restoration of the plasma membrane,...
3.8K


