A New Unc45a 5'utr Variant In Patients With Aagenaes Syndrome

IF 1.7 4区 生物学 Q3 GENETICS & HEREDITY American Journal of Medical Genetics Part A Pub Date : 2025-01-30 DOI:10.1002/ajmg.a.64004
Turkan Turkut Tan, Yusuf Can Dogan, Zehra Burcu Yilmaz, Enise Avci Durmusalioglu, Ezgi Oguz, Durdugul Emecen Ayyildiz, Esra Isik, Sema Aydogdu, Ozgur Cogulu, Tahir Atik
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Abstract

Aagenaes syndrome, also known as lymphoedema cholestasis syndrome 1 (LCS1), is a rare autosomal recessive disorder characterized by neonatal cholestasis and chronic lymphedema, primarily affecting the lower extremities. The genetic basis for this syndrome was recently linked to a variant in the 5′-untranslated region (5’-UTR) of the UNC45A gene, located on chromosome 15q. This study aimed to identify the genetic mutations associated with Aagenaes syndrome in two siblings and to explore their clinical implications. Whole-exome sequencing (WES) was conducted on two siblings with neonatal cholestasis and lymphedema. WES identified a single base pair change in the 5′-untranslated region (5’-UTR) of the UNC45A gene (c.-88G>A) in both siblings. Additionally, both were heterozygous for an exonic loss-of-function variant (c.1591C>T; p.Arg531Ter) in UNC45A. Clinically, both siblings presented with neonatal cholestasis and lymphedema; however, one sibling developed severe liver failure, requiring a liver transplant. Despite carrying the same variants, the clinical outcomes differed between the two patients. The identification of a novel 5’-UTR variant (c.-88G>A), along with an exonic variant in UNC45A, expands the genetic and clinical understanding of Aagenaes syndrome. This study confirms the involvement of the 5’-UTR region of UNC45A in the disease pathogenesis, while demonstrating that Aagenaes syndrome is not exclusively associated with the previously reported c.-98G>T variant found in Norwegian cases. These findings underscore the importance of genetic screening for accurate diagnosis and management of Aagenaes syndrome and provide new insights into the critical regulatory role of the 5’-UTR in disease development. Further research is needed to elucidate the mechanisms underlying phenotypic variability in this rare disorder. Evaluation of mRNA and protein levels would have been valuable to better understand the functional effects of these variants; however, due to current resource constraints, such studies could not be conducted.

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阿格奈斯综合征患者中一种新的unc45a5 'utr变异。
阿格奈斯综合征,又称淋巴水肿胆汁淤积综合征1 (LCS1),是一种罕见的常染色体隐性遗传病,以新生儿胆汁淤积和慢性淋巴水肿为特征,主要影响下肢。该综合征的遗传基础最近与位于15q染色体上的UNC45A基因5'-非翻译区(5'-UTR)的变异有关。本研究旨在确定两个兄弟姐妹中与阿格奈斯综合征相关的基因突变,并探讨其临床意义。对两名患有新生儿胆汁淤积和淋巴水肿的兄弟姐妹进行了全外显子组测序(WES)。WES在两个兄弟姐妹中发现了UNC45A基因(c - 88g > a)的5'-非翻译区(5'-UTR)的单个碱基对变化。此外,对于外显子功能缺失变体(c.1591C >t;p.Arg531Ter) in UNC45A。临床表现为新生儿胆汁淤积和淋巴水肿;然而,一个兄弟姐妹患上了严重的肝功能衰竭,需要肝移植。尽管携带相同的变异,两名患者的临床结果却不同。新的5'-UTR变异(c - 88g > a)的鉴定,以及UNC45A的外显子变异,扩大了对阿格奈斯综合征的遗传和临床认识。本研究证实了UNC45A的5'-UTR区域参与疾病发病机制,同时表明阿格奈斯综合征并不完全与先前报道的挪威病例中发现的c - 98g >T变异相关。这些发现强调了基因筛查对于准确诊断和管理Aagenaes综合征的重要性,并为5'-UTR在疾病发展中的关键调控作用提供了新的见解。需要进一步的研究来阐明这种罕见疾病的表型变异机制。评估mRNA和蛋白质水平对于更好地理解这些变异的功能影响是有价值的;但是,由于目前的资源限制,无法进行这种研究。
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来源期刊
CiteScore
3.50
自引率
5.00%
发文量
432
审稿时长
2-4 weeks
期刊介绍: The American Journal of Medical Genetics - Part A (AJMG) gives you continuous coverage of all biological and medical aspects of genetic disorders and birth defects, as well as in-depth documentation of phenotype analysis within the current context of genotype/phenotype correlations. In addition to Part A , AJMG also publishes two other parts: Part B: Neuropsychiatric Genetics , covering experimental and clinical investigations of the genetic mechanisms underlying neurologic and psychiatric disorders. Part C: Seminars in Medical Genetics , guest-edited collections of thematic reviews of topical interest to the readership of AJMG .
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