MIR96 (gene): Difference between revisions

Jump to navigation Jump to search
m (Bot: HTTP→HTTPS)
 
imported>Jmertel23
m (wikilinks added and "unlinked" tag removed)
 
Line 1: Line 1:
{{Underlinked|date=June 2016}}
{{Infobox_gene}}
{{Infobox_gene}}


'''MicroRNA 96''' is a [[protein]] that in humans is encoded by the MIR96 [[gene]].
'''MicroRNA 96''' is a [[protein]] that in humans is encoded by the MIR96 [[gene]].<ref name="entrez">
<ref name="entrez">
{{cite web
{{cite web
| title = Entrez Gene: MicroRNA 96
| title = Entrez Gene: MicroRNA 96
Line 12: Line 10:
==Function==
==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.
[[MicroRNA|microRNAs]] (miRNAs) are short (20-24 nt) [[Non-coding RNA|non-coding RNAs]] that are involved in post-transcriptional regulation of [[gene expression]] in [[Multicellular organism|multicellular organisms]] by affecting both the stability and [[Translation (biology)|translation]] of mRNAs. miRNAs are transcribed by [[RNA polymerase II]] as part of capped and polyadenylated [[Primary transcript|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 mRNA|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 ==
== References ==

Latest revision as of 14:17, 5 February 2018

VALUE_ERROR (nil)
Identifiers
Aliases
External IDsGeneCards: [1]
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

n/a

n/a

RefSeq (protein)

n/a

n/a

Location (UCSC)n/an/a
PubMed searchn/an/a
Wikidata
View/Edit Human

MicroRNA 96 is a protein that in humans is encoded by the MIR96 gene.[1]

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. "Entrez Gene: MicroRNA 96". Retrieved 2016-04-10.

Further reading

  • Mencía A, Modamio-Høybjør S, Redshaw N, Morín M, Mayo-Merino F, Olavarrieta L, Aguirre LA, del Castillo I, Steel KP, Dalmay T, Moreno F, Moreno-Pelayo MA (2009). "Mutations in the seed region of human miR-96 are responsible for nonsyndromic progressive hearing loss". Nat. Genet. 41 (5): 609–13. doi:10.1038/ng.355. PMID 19363479.

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