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MicroRNA: Biogenesis, Function and Role in Cancer

2010· article· en· 1,835 citations· W2141549067 on OpenAlex· 10.2174/138920210793175895

Why is this work in the frame?

A frame that forgets how it found something cannot be audited. These are the routes that admitted this work.

Canadian affiliationAn author listed a Canadian institution. This is the only route the usual frame has.

Machine scores (provisional)

Baseline scores from an immature model (maturity gate not passed, 7 training rounds). Scores rank; they never assert a category.

The two teacher heads of the student model, read on this work. A score orders the frame for review; it never asserts a category, and the validation status ships verbatim with every row.

Opus teacher head0.010
GPT teacher head0.255
Teacher spread
0.246 · how far apart the two teachers sit on this one work
Validation status
score_only:v0-immature-baseline · verbatim from the scoring run: score_only means the number may rank works, and no category label ships from it

Abstract

MicroRNAs are small, highly conserved non-coding RNA molecules involved in the regulation of gene expression. MicroRNAs are transcribed by RNA polymerases II and III, generating precursors that undergo a series of cleavage events to form mature microRNA. The conventional biogenesis pathway consists of two cleavage events, one nuclear and one cytoplasmic. However, alternative biogenesis pathways exist that differ in the number of cleavage events and enzymes responsible. How microRNA precursors are sorted to the different pathways is unclear but appears to be determined by the site of origin of the microRNA, its sequence and thermodynamic stability. The regulatory functions of microRNAs are accomplished through the RNA-induced silencing complex (RISC). MicroRNA assembles into RISC, activating the complex to target messenger RNA (mRNA) specified by the microRNA. Various RISC assembly models have been proposed and research continues to explore the mechanism(s) of RISC loading and activation. The degree and nature of the complementarity between the microRNA and target determine the gene silencing mechanism, slicer-dependent mRNA degradation or slicer-independent translation inhibition. Recent evidence indicates that P-bodies are essential for microRNA-mediated gene silencing and that RISC assembly and silencing occurs primarily within P-bodies. The P-body model outlines microRNA sorting and shuttling between specialized P-body compartments that house enzymes required for slicer – dependent and – independent silencing, addressing the reversibility of these silencing mechanisms. Detailed knowledge of the microRNA pathways is essential for understanding their physiological role and the implications associated with dysfunction and dysregulation. Keywords: MicroRNA, RNA interference (RNAi), Post-transcriptional gene regulation, Cancer, interference, Post-transcriptional, Biogenesis, RNA polymerases, RISC, P-bodies, Caenorhabditis elegans, (tRNA), (rRNA), (siRNA), (snoRNA), dsRNA, junk DNA, DNA methylation, DGCR8, (TRBP), (PACT), RNA Helicase A, Ago2, eIF2C2, Dicer, TRBP, PACT, (PKR), G:U wobble, Dcp1, Dcp2, RNA degradation, (HMGA2), CLL, MiR-21, PTEN, TPM1, miR-17-92, E2Fs, apoptosis, E2F3, qRT-PCR

Fetched live from OpenAlex and de-inverted. Abstracts are not stored in this database: the inverted indexes are 8.6 GB of the frame’s 9.3 GB of text, and the host has 13 GB free.

The record

Venue
Current Genomics
Topic
MicroRNA in disease regulation
Field
Biochemistry, Genetics and Molecular Biology
Canadian institutions
Dalhousie University
Funders
Keywords
Gene silencingmicroRNAArgonauteRNA-induced silencing complexBiologyCell biologyDicerRNASmall RNARNA silencingRNA interferenceComputational biologyGeneticsGeneNon-coding RNA
Has abstract in OpenAlex
yes