Graduate School of Interdisciplinary Science and Engineering in Health Systems, Okayama University, Okayama 700-8558, Japan.
Department of Ophthalmology, Okayama University Hospital, Okayama 700-8558, Japan.
Int J Mol Sci. 2022 Aug 3;23(15):8626. doi: 10.3390/ijms23158626.
Idiopathic superior oblique muscle palsy is a major type of paralytic, non-comitant strabismus and presents vertical and cyclo-torsional deviation of one eye against the other eye, with a large vertical fusion range and abnormal head posture such as head tilt. Genetic background is considered to play a role in its development, as patients with idiopathic superior oblique muscle palsy have varying degrees of muscle hypoplasia and, rarely, the complete absence of the muscle, that is, aplasia. In this study, whole genome sequencing was performed, and single nucleotide variations and short insertions/deletions (SNVs/InDels) were annotated in two patients each in three small families (six patients in total) with idiopathic superior oblique muscle palsy, in addition to three normal individuals in one family. At first, linkage analysis was carried out in the three families and SNVs/InDels in chromosomal loci with negative LOD scores were excluded. Next, SNVs/InDels shared by the six patients, but not by the three normal individuals, were chosen. SNVs/InDels were further narrowed down by choosing low-frequency (<1%) or non-registered SNVs/InDels in four databases for the Japanese population, and then by choosing SNVs/InDels with functional influence, leading to one candidate gene, SSTR5-AS1 in chromosome 16. The six patients were heterozygous for 13-nucleotide deletion in SSTR5-AS1, except for one homozygous patient, while the three normal individuals were wild type. Targeted polymerase chain reaction (PCR) and direct sequencing of PCR products confirmed the 13-nucleotide deletion in SSTR5-AS1. In the face of newly-registered SSTR5-AS1 13-nucleotide deletion at a higher frequency in a latest released database for the Japanese population, the skipping of low-frequency and non-registration sorting still resulted in only 13 candidate genes including SSTR5-AS1 as common variants. The skipping of linkage analysis also led to the same set of 13 candidate genes. Different testing strategies that consisted of linkage analysis and simple unintentional bioinformatics could reach candidate genes in three small families with idiopathic superior oblique muscle palsy.
特发性上斜肌麻痹是一种主要的麻痹性、非协同性斜视,表现为一眼相对于另一眼的垂直和回旋扭转偏斜,具有较大的垂直融合范围和异常的头位,如头倾斜。遗传背景被认为在其发展中起作用,因为特发性上斜肌麻痹患者的肌肉有不同程度的发育不良,并且很少出现肌肉完全缺失,即发育不全。在这项研究中,对三个小家族(共 6 名患者)中的每两名患者进行了全基因组测序,并对 3 名正常个体进行了注释,除了一个家族中的 3 名正常个体。首先,在三个家族中进行了连锁分析,并排除了染色体位置上具有负 LOD 评分的 SNVs/InDels。接下来,选择了 6 名患者共有的 SNVs/InDels,但 3 名正常个体没有。通过选择 4 个日本人群数据库中的低频(<1%)或未注册的 SNVs/InDels,进一步缩小了 SNVs/InDels 的范围,然后选择具有功能影响的 SNVs/InDels,导致一个候选基因,16 号染色体上的 SSTR5-AS1。除了一名纯合患者外,其余 6 名患者的 SSTR5-AS1 均为 13 核苷酸缺失杂合子,而 3 名正常个体均为野生型。目标聚合酶链反应(PCR)和 PCR 产物的直接测序证实了 SSTR5-AS1 中的 13 核苷酸缺失。在最新发布的日本人群数据库中,SSTR5-AS1 13 核苷酸缺失的新注册频率较高的情况下,通过跳过低频和非注册排序,仍然只有 13 个候选基因,包括 SSTR5-AS1 作为常见变体。连锁分析的跳过也导致了相同的 13 个候选基因集。包含连锁分析和简单非故意生物信息学的不同测试策略,可以在三个特发性上斜肌麻痹的小家族中找到候选基因。