Haviland Isabel, Hector Ralph D, Swanson Lindsay C, Verran Aubrie Soucy, Sherrill Emma, Frazier Zoë, Denny AnneMarie M, Lucash Jenna, Zhang Bo, Dubbs Holly A, Marsh Eric D, Weisenberg Judith L, Leonard Helen, Crippa Milena, Cogliati Francesca, Russo Silvia, Suter Bernhard, Rajaraman Rajsekar, Percy Alan K, Schreiber John M, Demarest Scott, Benke Timothy A, Chopra Maya, Yu Timothy W, Olson Heather E
Department of Neurology, Boston Children's Hospital, Boston, Massachusetts, USA.
Rosamund Stone Zander Translational Neuroscience Center, Boston Children's Hospital, Harvard Medical School, Boston, Massachusetts, USA.
Am J Med Genet A. 2025 Jan;197(1):e63843. doi: 10.1002/ajmg.a.63843. Epub 2024 Aug 28.
Pathogenic variants in the cyclin-dependent kinase-like 5 (CDKL5) gene are associated with CDKL5 deficiency disorder (CDD), a severe X-linked developmental and epileptic encephalopathy. Deletions affecting the 5' untranslated region (UTR) of CDKL5, which involve the noncoding exon 1 and/or alternatively spliced first exons (exons 1a-e), are uncommonly reported. We describe genetic and phenotypic characteristics for 15 individuals with CDKL5 partial gene deletions affecting the 5' UTR. All individuals presented characteristic features of CDD, including medically refractory infantile-onset epilepsy, global developmental delay, and visual impairment. We performed RNA sequencing on fibroblast samples from three individuals with small deletions involving exons 1 and/or 1a/1b only. Results demonstrated reduced CDKL5 mRNA expression with no evidence of expression from alternatively spliced first exons. Our study broadens the genotypic spectrum for CDD by adding to existing evidence that deletions affecting the 5' UTR of the CDKL5 gene are associated with the disorder. We propose that smaller 5' UTR deletions may require additional molecular testing approaches such as RNA sequencing to determine pathogenicity.
细胞周期蛋白依赖性激酶样5(CDKL5)基因的致病性变异与CDKL5缺陷障碍(CDD)相关,CDD是一种严重的X连锁发育性和癫痫性脑病。影响CDKL5 5'非翻译区(UTR)的缺失,涉及非编码外显子1和/或选择性剪接的首个外显子(外显子1a - e),报道较少。我们描述了15例影响5'UTR的CDKL5部分基因缺失个体的遗传和表型特征。所有个体均表现出CDD的特征性表现,包括药物难治性婴儿期癫痫、全面发育迟缓以及视力障碍。我们对仅涉及外显子1和/或1a/1b小缺失的3例个体的成纤维细胞样本进行了RNA测序。结果显示CDKL5 mRNA表达降低,且没有证据表明存在选择性剪接首个外显子的表达。我们的研究通过补充现有证据,即影响CDKL5基因5'UTR的缺失与该疾病相关,拓宽了CDD的基因型谱。我们提出,较小的5'UTR缺失可能需要额外的分子检测方法,如RNA测序,以确定致病性。