Growth and Development Group, Vall d'Hebron Research Institute (VHIR), Hospital Universitari Vall d'Hebron, Barcelona, Spain.
Pediatrics, Obstetrics and Gynecology and Preventive Medicine Department, Universitat Autònoma de Barcelona, Barcelona, Spain.
Front Endocrinol (Lausanne). 2022 Oct 11;13:957969. doi: 10.3389/fendo.2022.957969. eCollection 2022.
The palmitoylation of the Hedgehog (Hh) family of morphogens, named sonic hedgehog (SHH), desert hedgehog (DHH), and Indian hedgehog (IHH), is crucial for effective short- and long-range signaling. The hedgehog acyltransferase (HHAT) attaches the palmitate molecule to the Hh; therefore, variants in cause a broad spectrum of phenotypes. A missense novel variant c.1001T>A/p.(Met334Lys) was described in a patient first referred for a 46,XY different sexual development with partial gonadal dysgenesis but with microcephaly, eye defects, and distal phalangeal hypoplasia of both thumbs. The analysis of the variant predicted an affectation of the nearest splicing site. Thus, minigene studies were carried out, which demonstrated that the variant does not affect the splicing. Subsequent protein studies supported the pathogenicity of the variant, and, in conclusion, this was considered the cause of the patient's phenotype.
Hedgehog(Hh)家族形态发生素的棕榈酰化,被命名为 sonic hedgehog(SHH)、desert hedgehog(DHH)和 Indian hedgehog(IHH),对于有效进行短程和长程信号传递至关重要。Hedgehog 酰基转移酶(HHAT)将棕榈酸分子附着到 Hh 上;因此, 中的变体导致广泛的表型。在一个首次因 46,XY 不同性别发育且伴有部分性腺发育不全但伴有小头畸形、眼部缺陷和双侧拇指远节指骨发育不良的患者中描述了一种错义 新型变体 c.1001T>A/p.(Met334Lys)。对变体的 分析预测了最近的剪接位点受到影响。因此,进行了 minigene 研究,结果表明该变体不影响剪接。随后的蛋白质 研究支持该变体的致病性,因此,该变体被认为是患者表型的原因。