Whitman Mary C, Engle Elizabeth C
F.M. Kirby Neurobiology Center, Boston Children's Hospital, Boston, MA 02115, USA.
Department of Ophthalmology, Boston Children's Hospital, Boston, MA 02115, USA.
Hum Mol Genet. 2017 Aug 1;26(R1):R37-R44. doi: 10.1093/hmg/ddx168.
Unraveling the genetics of the paralytic strabismus syndromes known as congenital cranial dysinnervation disorders (CCDDs) is both informing physicians and their patients and broadening our understanding of development of the ocular motor system. Genetic mutations underlying ocular CCDDs alter either motor neuron specification or motor nerve development, and highlight the importance of modulations of cell signaling, cytoskeletal transport, and microtubule dynamics for axon growth and guidance. Here we review recent advances in our understanding of two CCDDs, congenital fibrosis of the extraocular muscles (CFEOM) and Duane retraction syndrome (DRS), and discuss what they have taught us about mechanisms of axon guidance and selective vulnerability. CFEOM presents with congenital ptosis and restricted eye movements, and can be caused by heterozygous missense mutations in the kinesin motor protein KIF21A or in the β-tubulin isotypes TUBB3 or TUBB2B. CFEOM-causing mutations in these genes alter protein function and result in axon growth and guidance defects. DRS presents with inability to abduct one or both eyes. It can be caused by decreased function of several transcription factors critical for abducens motor neuron identity, including MAFB, or by heterozygous missense mutations in CHN1, which encodes α2-chimaerin, a Rac-GAP GTPase that affects cytoskeletal dynamics. Examination of the orbital innervation in mice lacking Mafb has established that the stereotypical misinnervation of the lateral rectus by fibers of the oculomotor nerve in DRS is secondary to absence of the abducens nerve. Studies of a CHN1 mouse model have begun to elucidate mechanisms of selective vulnerability in the nervous system.
揭示被称为先天性颅神经支配障碍(CCDDs)的麻痹性斜视综合征的遗传学,既能为医生及其患者提供信息,又能拓宽我们对眼球运动系统发育的理解。导致眼部CCDDs的基因突变会改变运动神经元的特化或运动神经的发育,并突出了细胞信号传导、细胞骨架运输和微管动力学调节对轴突生长和导向的重要性。在这里,我们回顾了我们对两种CCDDs,即先天性眼外肌纤维化(CFEOM)和杜安退缩综合征(DRS)的理解的最新进展,并讨论它们教会了我们哪些关于轴突导向和选择性易损性的机制。CFEOM表现为先天性上睑下垂和眼球运动受限,可由驱动蛋白运动蛋白KIF21A或β-微管蛋白亚型TUBB3或TUBB2B中的杂合错义突变引起。这些基因中导致CFEOM的突变会改变蛋白质功能,并导致轴突生长和导向缺陷。DRS表现为一只或两只眼睛外展无力。它可能由对展神经运动神经元身份至关重要的几种转录因子功能下降引起,包括MAFB,或由CHN1中的杂合错义突变引起,CHN1编码α2-嵌合蛋白,一种影响细胞骨架动力学的Rac-GAP GTP酶。对缺乏Mafb的小鼠的眼眶神经支配进行检查后发现,DRS中动眼神经纤维对外直肌的典型错误支配是展神经缺失的继发结果。对CHN1小鼠模型的研究已经开始阐明神经系统中选择性易损性的机制。