Abreu Ana Paula, Macedo Delanie B, Brito Vinicius N, Kaiser Ursula B, Latronico Ana Claudia
Division of EndocrinologyDiabetes and Hypertension, Harvard Medical School, Brigham and Women's Hospital, Boston, Massachusetts, USAUnidade de Endocrinologia do DesenvolvimentoDisciplina de Endocrinologia e Metabologia, Laboratório de Hormônios e Genética Molecular, LIM 42, Hospital das Clínicas, Faculdade de Medicina da Universidade de São Paulo, Avenida Dr Enéas de Carvalho Aguiar, 255, 7° andar, sala 7037, CEP: 05403-900, São Paulo, Brazil.
Division of EndocrinologyDiabetes and Hypertension, Harvard Medical School, Brigham and Women's Hospital, Boston, Massachusetts, USAUnidade de Endocrinologia do DesenvolvimentoDisciplina de Endocrinologia e Metabologia, Laboratório de Hormônios e Genética Molecular, LIM 42, Hospital das Clínicas, Faculdade de Medicina da Universidade de São Paulo, Avenida Dr Enéas de Carvalho Aguiar, 255, 7° andar, sala 7037, CEP: 05403-900, São Paulo, Brazil
J Mol Endocrinol. 2015 Jun;54(3):R131-9. doi: 10.1530/JME-14-0315.
Pubertal timing is influenced by complex interactions among genetic, nutritional, environmental, and socioeconomic factors. The role of MKRN3, an imprinted gene located in the Prader-Willi syndrome critical region (chromosome 15q11-13), in pubertal initiation was first described in 2013 after the identification of deleterious MKRN3 mutations in five families with central precocious puberty (CPP) using whole-exome sequencing analysis. Since then, additional loss-of-function mutations of MKRN3 have been associated with the inherited premature sexual development phenotype in girls and boys from different ethnic groups. In all of these families, segregation analysis clearly demonstrated autosomal dominant inheritance with complete penetrance, but with exclusive paternal transmission, consistent with the monoallelic expression of MKRN3 (a maternally imprinted gene). Interestingly, the hypothalamic Mkrn3 mRNA expression pattern in mice correlated with a putative inhibitory input on puberty initiation. Indeed, the initiation of puberty depends on a decrease in factors that inhibit the release of GnRH combined with an increase in stimulatory factors. These recent human and animal findings suggest that MKRN3 plays an inhibitory role in the reproductive axis to represent a new pathway in pubertal regulation.
青春期启动时间受遗传、营养、环境和社会经济因素之间复杂相互作用的影响。MKRN3是一种位于普拉德-威利综合征关键区域(染色体15q11 - 13)的印记基因,2013年,通过全外显子组测序分析在五个中枢性性早熟(CPP)家庭中鉴定出有害的MKRN3突变后,其在青春期启动中的作用首次被描述。从那时起,MKRN3的其他功能丧失突变与来自不同种族的女孩和男孩的遗传性性早熟表型相关。在所有这些家庭中,分离分析清楚地表明其为常染色体显性遗传且具有完全外显率,但仅通过父系遗传,这与MKRN3(一个母系印记基因)的单等位基因表达一致。有趣的是,小鼠下丘脑Mkrn3 mRNA表达模式与青春期启动的假定抑制性输入相关。实际上,青春期的启动取决于抑制促性腺激素释放激素(GnRH)释放的因子减少以及刺激性因子增加。这些最新的人类和动物研究结果表明,MKRN3在生殖轴中起抑制作用,代表了青春期调节的一条新途径。