Lederbauer Johannes, Das Sarada, Piton Amelie, Lessel Davor, Kreienkamp Hans-Jürgen
Institute of Human Genetics, University Hospital Salzburg, Paracelsus Medical University, Salzburg, Austria.
Institute of Human Genetics, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
Front Mol Neurosci. 2024 Aug 1;17:1414949. doi: 10.3389/fnmol.2024.1414949. eCollection 2024.
Neurodevelopmental disorders (NDDs) represent a large group of disorders with an onset in the neonatal or early childhood period; NDDs include intellectual disability (ID), autism spectrum disorders (ASD), attention deficit hyperactivity disorders (ADHD), seizures, various motor disabilities and abnormal muscle tone. Among the many underlying Mendelian genetic causes for these conditions, genes coding for proteins involved in all aspects of the gene expression pathway, ranging from transcription, splicing, translation to the eventual RNA decay, feature rather prominently. Here we focus on two large families of RNA helicases (DEAD- and DExH-box helicases). Genetic variants in the coding genes for several helicases have recently been shown to be associated with NDD. We address genetic constraints for helicases, types of pathological variants which have been discovered and discuss the biological pathways in which the affected helicase proteins are involved.
神经发育障碍(NDDs)是一大类在新生儿期或幼儿期发病的疾病;NDDs包括智力残疾(ID)、自闭症谱系障碍(ASD)、注意力缺陷多动障碍(ADHD)、癫痫、各种运动障碍和异常肌张力。在这些疾病的众多潜在孟德尔遗传病因中,编码参与基因表达途径各个方面(从转录、剪接、翻译到最终的RNA降解)的蛋白质的基因显得尤为突出。在这里,我们重点关注两大类RNA解旋酶(DEAD盒和解旋酶盒解旋酶)。最近有研究表明,几种解旋酶编码基因中的遗传变异与NDD有关。我们探讨了解旋酶的遗传限制、已发现的病理变异类型,并讨论了受影响的解旋酶蛋白所涉及的生物学途径。