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MIR503

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This is an old revision of this page, as edited by Ffffrr (talk | contribs) at 09:15, 27 March 2022 (Importing Wikidata short description: "Non-coding RNA in the species Homo sapiens" (Shortdesc helper)). The present address (URL) is a permanent link to this revision, which may differ significantly from the current revision.

MIR503
Identifiers
AliasesMIR503, MIRN503, hsa-mir-503, mir-503, microRNA 503
External IDsOMIM: 300865; GeneCards: MIR503; OMA:MIR503 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

n/a

n/a

RefSeq (protein)

n/a

n/a

Location (UCSC)Chr X: 134.55 – 134.55 Mbn/a
PubMed search[2]n/a
Wikidata
View/Edit Human

MicroRNA 503 is a non-coding RNA molecule that in humans is encoded by the MIR503 gene. [3]

Function

microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding.

The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products.

The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop.

References

  1. ^ a b c GRCh38: Ensembl release 89: ENSG00000208005Ensembl, May 2017
  2. ^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  3. ^ "Entrez Gene: MicroRNA 503". Retrieved 2017-05-30.

Further reading

This article incorporates text from the United States National Library of Medicine, which is in the public domain.