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Small Cajal body-specific RNA 9 (SCARNA9)

Target
SCARNA9
Molecular classification
scaRNA (small Cajal body-specific RNA), long non-coding RNA (lncRNA)
01

Overview

Small Cajal body-specific RNA 9 (SCARNA9) is a member of the scaRNA family, a class of small non-coding RNAs localized to Cajal bodies within the nucleus[3][1][5]. These RNAs serve as guide RNAs for the site-specific modification of spliceosomal snRNAs, particularly U2, by directing enzymes responsible for pseudouridylation and 2'-O-methylation. SCARNA9 is processed by the Drosha-DGCR8 microprocessor complex, resulting in fragments such as mgU2-19 and mgU2-30, which contribute to snRNA maturation[2]. As lncC11orf54-1, SCARNA9 has been implicated in neuroinflammatory response via activation of NF-kappaB signaling[4]. SCARNA9 is not considered a classical drug target like a receptor or enzyme, and no drugs are known to interact with it. It belongs to the molecular family of small non-coding RNAs that orchestrate RNA modification, essential for spliceosome function and proper cell regulation. Currently, there are no direct disease biomarker or safety concerns associated with SCARNA9.

Other names
mgU2-19/30Z32lncC11orf54-1mgU2-19/30 scaRNASmall Cajal body-specific RNA 9SCARNA9
02

Mechanism of action

Not applicable for drugs, but mechanistically, SCARNA9 acts by guiding enzymes to sites of pseudouridylation and 2'-O-methylation on spliceosomal snRNAs through base-pairing interactions

03

Biological functions

Guide RNA for site-specific modification of small nuclear RNAs (snRNAs), especially U2 snRNAInvolved in biogenesis and maturation of spliceosomal snRNAs by guiding pseudouridylation and 2′-O-methylationRegulation of rRNA modification, possibly via regulatory RNPs (regRNPs)Modulation of neuroinflammatory responses via activation of NF-kappaB signaling (lncC11orf54-1 alias)
04

Disease associations

Neuroinflammatory disease: lncC11orf54-1 modulates neuroinflammatory responses, especially during meningitic Escherichia coli infectionOther: Given its role in RNA modification and cell regulation, disturbances could hypothetically contribute to splicing or RNA-related diseases, but no specific common disease associations are documented.
05

Safety considerations

None reported. No therapeutic interventions target SCARNA9 directly
06

Interacting drugs

None reported. No drugs are known to selectively target SCARNA9
07

Biomarkers

None established for patient selection or efficacy monitoring

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