ESPE2024 Free Communications Multisystem Endocrine Disorders (6 abstracts)
Using sno-lncRNAs as potential markers for Prader-Willi syndrome diagnosis
Chaochun Zou , Jiu-Ru Sun , Liang-Zhong Yang , Yang-Li Dai , Huang Wu , Siqi Li , Yifeng Xu , Youkui Huang , Hao Wu , Zheng Shen & Ling-Ling Chen
Hangzhou, Zhejiang, China
The genetic disorder Prader-Willi syndrome (PWS) is mainly caused by the loss of multiple paternally expressed genes in chromosome 15q11-q13 (the PWS region). Early diagnosis of PWS is essential for timely treatment, leading to effectively easing some clinical symptoms. Molecular approaches for PWS diagnosis at the DNA level are available, but the diagnosis of PWS at the RNA level has been limited. Here, we show that a cluster of paternally transcribed snoRNA-ended long noncoding RNAs (sno-lncRNAs, sno-lncRNA1-5) derived from the SNORD116 locus in the PWS region can serve as diagnostic markers. In particular, quantification analysis has revealed that 6,000 copies of sno-lncRNA3 are present in 1 μL whole blood samples from non-PWS individuals. sno-lncRNA3 is absent in all examined whole blood samples of 8 PWS individuals compared to 42 non-PWS individuals and dried blood samples of 35 PWS individuals compared to 24 non-PWS individuals. Further developing a new CRISPR-MhdCas13c system for RNA detection with a sensitivity of 10 molecules per μL has ensured sno-lncRNA3 detection in non-PWS, but not PWS individuals. Together, we suggest that the absence of sno-lncRNA3 represents a potential marker for PWS diagnosis that can be detected by both RT-qPCR and CRISPR-MhdCas13c systems with only microlitre amount of blood samples. Such an RNA-based sensitive and convenient approach may facilitate the early detection of PWS.
Keywords: CRISPR-Mhdcas13c; Prader-Willi syndrome; RNA detection; Sno-lncRNA3; Sno-lncRNAs; diagnostic marker; dried blood spot; whole blood samples.
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