Research Centre for Medical Genetics, 115522 Moscow, Russia.
Republican Children's Clinical Hospital, 362003 Vladikavkaz, Russia.
Int J Mol Sci. 2023 Feb 24;24(5):4515. doi: 10.3390/ijms24054515.
North Caucasus has always been a residence of a lot of different authentic ethnic groups speaking different languages and still living their traditional lifestyle. The diversity appeared to be reflected in the accumulation of different mutations causing common inherited disorders. X-linked ichthyosis represents the second most common form of genodermatoses after ichthyosis vulgaris. Eight patients from three unrelated families of different ethnic origin, Kumyk, Turkish Meskhetians, and Ossetian, with X-linked ichthyosis from the North Caucasian Republic of North Ossetia-Alania were examined. NGS technology was implied for searching for disease-causing variants in one of the index patients. Known pathogenic hemizygous deletion in the short arm of chromosome X encompassing the STS gene was defined in the Kumyk family. A further analysis allowed us to establish that likely the same deletion was a cause of ichthyosis in a family belonging to the Turkish Meskhetians ethnic group. In the Ossetian family, a likely pathogenic nucleotide substitution in the STS gene was defined; it segregated with the disease in the family. We molecularly confirmed XLI in eight patients from three examined families. Though in two families, Kumyk and Turkish Meskhetian, we revealed similar hemizygous deletions in the short arm of chromosome X, but their common origin was not likely. Forensic STR markers of the alleles carrying the deletion were defined to be different. However, here, common alleles haplotype is hard to track for a high local recombination rate. We supposed the deletion could arise as a de novo event in a recombination hot spot in the described and in other populations with a recurrent character. Defined here are the different molecular genetic causes of X-linked ichthyosis in families of different ethnic origins sharing the same residence place in the Republic of North Ossetia-Alania which could point to the existing reproductive barriers even inside close neighborhoods.
北高加索地区一直是许多不同民族的居住地,这些民族说着不同的语言,至今仍保持着传统的生活方式。这种多样性反映在导致常见遗传性疾病的不同突变的积累上。X 连锁鱼鳞病是继寻常型鱼鳞病之后第二常见的遗传性皮肤病。我们对来自北奥塞梯-阿兰共和国(俄罗斯北高加索联邦管区)的三个不同民族(库梅克族、土耳其麦斯赫蒂族和奥塞梯族)的三个无关家庭的 8 名 X 连锁鱼鳞病患者进行了检查。在一名索引患者中,我们应用 NGS 技术寻找致病变异。在库梅克家族中,发现了 X 染色体短臂上包含 STS 基因的已知致病半合子缺失。进一步的分析表明,土耳其麦斯赫蒂族的一个家族的鱼鳞病可能也是由相同的缺失引起的。在奥塞梯家族中,我们定义了 STS 基因中可能的致病核苷酸取代,该取代与家族中的疾病共分离。我们在三个被检查的家族的 8 名患者中分子证实了 XLI。尽管在两个家族,库梅克族和土耳其麦斯赫蒂族,我们发现了 X 染色体短臂上相似的半合子缺失,但它们的共同起源不太可能。携带缺失的等位基因的法医 STR 标记被定义为不同。然而,由于局部高重组率,共同的等位基因单倍型很难追踪。我们推测,在描述的和其他具有反复特征的人群中,缺失可能作为重组热点的新生事件发生。在北奥塞梯-阿兰共和国,我们确定了具有不同遗传起源的家庭中 X 连锁鱼鳞病的不同分子遗传原因,这可能表明即使在临近地区也存在生殖障碍。