Mio Catia, Baldan Federica, Damante Giuseppe
Dipartimento di Area Medica, Università degli Studi di Udine, Udine 33100, Italy.
Istituto di Genetica Medica, Azienda Sanitaria Universitaria Friuli Centrale, Udine 33100, Italy.
Genes Dis. 2022 Oct 11;10(5):2038-2048. doi: 10.1016/j.gendis.2022.10.001. eCollection 2023 Sep.
NK2 genes ( gene cluster in humans) encode for homeodomain-containing transcription factors that are conserved along the phylogeny. According to the most detailed classifications, vertebrate genes are classified into two distinct families, and . The former is constituted by and genes which are homologous to the gene; the latter includes and genes, which are homologous to the gene. Conservation of these genes is not only related to molecular structure and expression, but also to biological functions. In and vertebrates, NK2 genes share roles in the development of ventral regions of the central nervous system. In vertebrates, genes have a relevant role in the development of several other organs such as the thyroid, lung, and pancreas. Loss-of-function mutations in and are the monogenic cause of the brain-lung-thyroid syndrome and neonatal diabetes, respectively. Alterations in and genes may play a role in multifactorial diseases, autism spectrum disorder, and neural tube defects, respectively. , , and are expressed in various cancer types as either oncogenes or tumor suppressor genes. Several data indicate that evaluation of their expression in tumors has diagnostic and/or prognostic value.
NK2基因(人类基因簇)编码含同源结构域的转录因子,这些转录因子在系统发育过程中是保守的。根据最详细的分类,脊椎动物基因分为两个不同的家族,即 和 。前者由与 基因同源的 和 基因组成;后者包括与 基因同源的 和 基因。这些基因的保守性不仅与分子结构和表达有关,还与生物学功能有关。在 和脊椎动物中,NK2基因在中枢神经系统腹侧区域的发育中发挥作用。在脊椎动物中, 基因在甲状腺、肺和胰腺等其他几个器官的发育中具有重要作用。 和 的功能丧失突变分别是脑-肺-甲状腺综合征和新生儿糖尿病的单基因病因。 和 基因的改变可能分别在多因素疾病、自闭症谱系障碍和神经管缺陷中起作用。 、 和 在各种癌症类型中作为癌基因或肿瘤抑制基因表达。一些数据表明,评估它们在肿瘤中的表达具有诊断和/或预后价值。