MIR335 is a microRNA implicated in various cellular processes, and its deregulation has been observed in adipose-derived stem cells (ASCs) [PMC6053905]. This deregulation is associated with a disruption in the timely inactivation of the T gene, which is further linked to compromised lamin A interaction with the T locus, as evidenced by studies conducted on mutant induced pluripotent stem cells (iPS cells) [PMC6053905]. Additionally, MIR335 is among a group of microRNAs, including MIR24-2, MIR142, MIR490, and MIR296, that are present in extracellular vesicles (EVs) [PMC7287171]. These microRNAs are known to target genes that are predominantly involved in critical signaling and structural pathways within the cell such as "Ras protein signal transduction" and "Actin/microtubule cytoskeleton organization" [PMC7287171]. The presence of MIR335 within EVs suggests its potential role in intercellular communication and regulation of these pathways.
--------uguuu c A C U gu
ugag gggggUCA GAGCAAUAA GAAAAAUG uu c
|||| |||||||| ||||||||| |||||||| ||
acuc ccuCCAGU CUCGUUAUU CUUUUUgc aa a
acuuauaucguuu u C A c au
| Disease | Description | Category | PubMed ID |
|---|
| Accession | MIMAT0000765 |
| Description | Homo sapiens hsa-miR-335-5p mature miRNA |
| Sequence | 16 - UCAAGAGCAAUAACGAAAAAUGU - 38 |
| Evidence |
experimental
cloned [3-4] |
| Database links |
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| Predicted targets |
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| Accession | MIMAT0004703 |
| Description | Homo sapiens hsa-miR-335-3p mature miRNA |
| Sequence | 52 - UUUUUCAUUAUUGCUCCUGACC - 73 |
| Evidence |
experimental
cloned [3] |
| Database links |
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| Predicted targets |
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