Department of Clinical Genetics, Maastricht University Medical Center+, azM, Maastricht, 6202 AZ, The Netherlands.
Department of Genetics and Cell Biology, School for Oncology and Developmental Biology, GROW, FHML, Maastricht University, Maastricht, 6200 MD, The Netherlands.
Mol Psychiatry. 2019 Nov;24(11):1748-1768. doi: 10.1038/s41380-018-0065-x. Epub 2018 May 4.
RLIM, also known as RNF12, is an X-linked E3 ubiquitin ligase acting as a negative regulator of LIM-domain containing transcription factors and participates in X-chromosome inactivation (XCI) in mice. We report the genetic and clinical findings of 84 individuals from nine unrelated families, eight of whom who have pathogenic variants in RLIM (RING finger LIM domain-interacting protein). A total of 40 affected males have X-linked intellectual disability (XLID) and variable behavioral anomalies with or without congenital malformations. In contrast, 44 heterozygous female carriers have normal cognition and behavior, but eight showed mild physical features. All RLIM variants identified are missense changes co-segregating with the phenotype and predicted to affect protein function. Eight of the nine altered amino acids are conserved and lie either within a domain essential for binding interacting proteins or in the C-terminal RING finger catalytic domain. In vitro experiments revealed that these amino acid changes in the RLIM RING finger impaired RLIM ubiquitin ligase activity. In vivo experiments in rlim mutant zebrafish showed that wild type RLIM rescued the zebrafish rlim phenotype, whereas the patient-specific missense RLIM variants failed to rescue the phenotype and thus represent likely severe loss-of-function mutations. In summary, we identified a spectrum of RLIM missense variants causing syndromic XLID and affecting the ubiquitin ligase activity of RLIM, suggesting that enzymatic activity of RLIM is required for normal development, cognition and behavior.
RLIM,也称为 RNF12,是一种 X 连锁的 E3 泛素连接酶,作为 LIM 结构域转录因子的负调节剂,参与小鼠的 X 染色体失活(XCI)。我们报告了来自九个无关家庭的 84 名个体的遗传和临床发现,其中 8 名个体在 RLIM(环指 LIM 结构域相互作用蛋白)中存在致病性变异。共有 40 名受影响的男性患有 X 连锁智力障碍(XLID)和可变的行为异常,伴有或不伴有先天性畸形。相比之下,44 名杂合子女性携带者认知和行为正常,但有 8 名表现出轻微的身体特征。鉴定的所有 RLIM 变体都是错义变化,与表型共分离,并预测会影响蛋白功能。九个改变的氨基酸中有八个是保守的,位于与相互作用蛋白结合相关的结构域内或 C 末端 RING 指催化结构域内。体外实验表明,RLIM RING 指中的这些氨基酸变化会损害 RLIM 泛素连接酶的活性。在 rlim 突变斑马鱼的体内实验中,野生型 RLIM 挽救了斑马鱼 rlim 表型,而患者特异性错义 RLIM 变体未能挽救表型,因此可能是严重的功能丧失突变。总之,我们鉴定了一系列导致综合征性 XLID 的 RLIM 错义变体,并影响 RLIM 的泛素连接酶活性,表明 RLIM 的酶活性对于正常发育、认知和行为是必需的。