Laboratory of Muscle Stem Cells and Gene Regulation, National Institute of Arthritis, Musculoskeletal, and Skin Diseases, National Institutes of Health , Bethesda, Maryland.
School of Pharmacy and Pharmaceutical Sciences, Binghamton University, State University of New York , Binghamton New York.
Physiol Genomics. 2018 Sep 1;50(9):694-704. doi: 10.1152/physiolgenomics.00128.2017. Epub 2018 May 11.
Mutations in the lamin A/C ( LMNA) gene cause a broad range of clinical syndromes that show tissue-restricted abnormalities of post mitotic tissues, such as muscle, nerve, heart, and adipose tissue. Mutations in other nuclear envelope proteins cause clinically overlapping disorders. The majority of mutations are dominant single amino acid changes (toxic protein produced by the single mutant gene), and patients are heterozygous with both normal and abnormal proteins. Experimental support has been provided for different models of cellular pathogenesis in nuclear envelope diseases, including changes in heterochromatin formation at the nuclear membrane (epigenomics), changes in the timing of steps during terminal differentiation of cells, and structural abnormalities of the nuclear membrane. These models are not mutually exclusive and may be important in different cells at different times of development. Recent experiments using fusion proteins of normal and mutant lamin A/C proteins fused to a bacterial adenine methyltransferase (DamID) provided compelling evidence of mutation-specific perturbation of epigenomic imprinting during terminal differentiation. These gain-of-function properties include lineage-specific ineffective genomic silencing during exit from the cell cycle (heterochromatinization), as well as promiscuous initiation of silencing at incorrect places in the genome. To date, these findings have been limited to a few muscular dystrophy and lipodystrophy LMNA mutations but seem shared with a distinct nuclear envelope disease, emerin-deficient muscular dystrophy. The dominant-negative structural model and gain-of-function epigenomic models for distinct LMNA mutations are not mutually exclusive, and it is likely that both models contribute to aspects of the many complex clinical phenotypes observed.
核纤层蛋白 A/C(LMNA)基因突变可导致广泛的临床综合征,表现为有丝分裂后组织的组织受限异常,如肌肉、神经、心脏和脂肪组织。其他核包膜蛋白的突变可导致临床重叠的疾病。大多数突变是显性单氨基酸变化(由单个突变基因产生的毒性蛋白),患者为杂合子,同时具有正常和异常蛋白。核包膜疾病的细胞发病机制的不同模型已提供了实验支持,包括核膜上异染色质形成的变化(表观基因组学)、细胞终末分化过程中步骤的时间变化,以及核膜的结构异常。这些模型并非相互排斥,在不同的细胞和不同的发育时期可能很重要。最近使用正常和突变 LMNA 蛋白融合到细菌腺嘌呤甲基转移酶(DamID)的融合蛋白的实验提供了令人信服的证据,证明了终末分化过程中特定于突变的表观基因组印迹的改变。这些功能获得特性包括谱系特异性的基因组沉默无效,退出细胞周期(异染色质化),以及在基因组的错误位置启动沉默。迄今为止,这些发现仅限于少数肌营养不良症和脂肪营养不良症 LMNA 突变,但似乎与一种独特的核包膜疾病,即核纤层蛋白 A/C 基因突变相关的肌营养不良症。不同 LMNA 突变的显性负性结构模型和功能获得性表观基因组模型并非相互排斥,并且这两种模型都可能对观察到的许多复杂临床表型的某些方面做出贡献。