MIR145 | |||||||
---|---|---|---|---|---|---|---|
Identifiers | |||||||
Aliases | MIR145, microRNA 145, MIRN145, miR-145, miRNA145 | ||||||
External IDs | GeneCards: MIR145 | ||||||
Orthologs | |||||||
Species | Human | Mouse | |||||
Entrez |
|
|
|||||
Ensembl |
|
|
|||||
UniProt |
|
|
|||||
RefSeq (mRNA) |
|
|
|||||
RefSeq (protein) |
|
|
|||||
Location (UCSC) | Chr 5: 149.43 – 149.43 Mb | n/a | |||||
PubMed search | n/a | ||||||
|
mir-145 | |
---|---|
Conserved secondary structure of mir-145
|
|
Identifiers | |
Symbol | mir-145 |
Rfam | RF00675 |
miRBase family | MIPF0000079 |
Other data | |
RNA type | microRNA |
Domain(s) | Eukaryota; |
SO | {{{SO}}} |
n/a
n/a
n/a
n/a
n/a
n/a
n/a
n/a
In molecular biology, mir-145 microRNA is a short RNA molecule that in humans is encoded by the MIR145 gene. MicroRNAs function to regulate the expression levels of other genes by several mechanisms.
MicroRNAs are involved in down-regulation of a variety of target genes. Götte et al. have shown that experimental over-expression of mir-145 down-regulates the junctional cell adhesion molecule JAM-A as well as the actin bundling protein fascin. Larsson et al. showed that miR-145 targets the 3' UTR of the FLI1 gene, a finding that was later supported by Zhang et al.
miR-145 is hypothesised to be a tumor suppressor. miR-145 has been shown to be down-regulated in breast cancer. miR-145 is also involved in colon cancer and acute myeloid leukemia.