Biology:mir-127
| mir-127 | |
|---|---|
 miR-127 microRNA secondary structure and sequence conservation | |
| Identifiers | |
| Symbol | mir-127 |
| Rfam | RF00676 |
| miRBase family | MIPF0000080 |
| NCBI Gene | 406914 |
| HGNC | 31509 |
| OMIM | 611709 |
| Other data | |
| RNA type | microRNA |
| Domain(s) | Eukaryota; |
| PDB structures | PDBe |
mir-127 microRNA is a short non-coding RNA molecule with interesting overlapping gene structure. miR-127 functions to regulate the expression levels of genes involved in lung development, placental formation and apoptosis. Aberrant expression of miR-127 has been linked to different cancers.
Gene structure
pri-miR-127 is derived from a separate but overlapping conserved gene cluster coding for miR-433/127. miR-127 and miR-433 are overlapped in a 5'-3' direction.[1] Although the loci could be found on different chromosomes in different species, the structure has been conserved. In mammals including human, chimpanzee, horse, dog, monkey, rat, cow, and mouse, multiple sequence alignments (MSA) between miR-433 and miR127 have shown 95-100% similarity with a conserved distance between miR-433 and miR-127 of 986 to 1007 bp. Moreover, the upstream response elements in the miR-433/127 promoters, including estrogen related receptors response element (ERRE) have been conserved among above species. Data have suggested that that miR-433/127 loci may have evolved from a common gene of origin.[2]
Transcription regulation
Transcription factor binding sites positioned upstream of miRNA precursor play a role in regulating transcription. Activation of miR-127 and miR-433 promoters is mediated by estrogen-related receptor gamma (ERRgamma, NR3B3), which physically associates with their endogenous promoters. Inhibition is regulated by Small heterodimer partner (SHP), which acts in trans.[3] Although miR-127 and miR-433 have common regulatory elements, they have independent promoters and their differential expression pattern is observed.[4]
Functional roles
Down-regulation of the imprinted gene Rtl1
Rtl1 is a key gene in placenta formation and the loss or overexpression of Rlt1 have led to late-fetal or neonatal lethality in mice.[5] miR-127 is located near CpG islands in the imprinted region encoding rtl1 and is normally transcribed in an antisense orientation to the gene. Ectopic expression of miR-127 resulted in a reduction in Rtl1 expression in Human Hela cell and mouse Heppa-1.
Experiments performed in mice showed that Rtl1 was only transcribed from the paternal chromosome, while the maternal allele was degraded. miR-127 and miR-136 however, are only maternally expressed in the somatic cells and thus play a role in antisense regulation of Rtl1 imprinting. Aberrant methylation status of Rtl1 and miR-127 indicated that epigenetic programming is also involved in the process.[2]
Control of fetal lung development
miR-127 is highly expressed in late state of fetal development. A disruption to the system by overexpressing miR-127 in a fetal lung organ culture system resulted in defective development shown by a decrease in terminal bud counts and varied bud sizes.[6]
Role in disease
Diffuse large B-cell lymphoma
Upregulation of miR-127 caused a downregulation of B-cell lymphoma 6 protein, a proto-oncogene which is usually hypermutated in diffuse large B-cell lymphoma (DLCL).[7][8] Moreover, differential expression of miR-127 was detected in different type of DLCL. miR-127 levels were significantly higher in the testicular DLCL compared with the nodal and central nervous system DLCL, implying different biological entity of DLCL in different locations.[9]
Hepatocellular carcinoma
Inhibition of miR-127 expression is linked with Hepatocellular carcinoma. The mechanistic link was confirmed by a change in BCL6 protein, which is targeted by miR-127.[10]
See also
References
- ↑ Song G, Wang L (2008). Volff, Jean-Nicolas. ed. "MiR-433 and miR-127 arise from independent overlapping primary transcripts encoded by the miR-433-127 locus". PLOS ONE 3 (10): e3574. doi:10.1371/journal.pone.0003574. PMID 18974780.
- ↑ 2.0 2.1 Song G, Wang L (2009). Tora, Laszlo. ed. "A conserved gene structure and expression regulation of miR-433 and miR-127 in mammals". PLOS ONE 4 (11): e7829. doi:10.1371/journal.pone.0007829. PMID 19946636.
- ↑ "The orphan nuclear receptor SHP regulates PGC-1alpha expression and energy production in brown adipocytes". Cell Metab. 2 (4): 227–38. October 2005. doi:10.1016/j.cmet.2005.08.010. PMID 16213225.
- ↑ "Transcriptional mechanism for the paired miR-433 and miR-127 genes by nuclear receptors SHP and ERRgamma". Nucleic Acids Res. 36 (18): 5727–35. October 2008. doi:10.1093/nar/gkn567. PMID 18776219.
- ↑ "Role of retrotransposon-derived imprinted gene, Rtl1, in the feto-maternal interface of mouse placenta". Nat. Genet. 40 (2): 243–8. February 2008. doi:10.1038/ng.2007.51. PMID 18176565.
- ↑ "MicroRNA-127 modulates fetal lung development". Physiol. Genomics 37 (3): 268–78. May 2009. doi:10.1152/physiolgenomics.90268.2008. PMID 19439715.
- ↑ "MicroRNA expression profiles classify human cancers". Nature 435 (7043): 834–8. June 2005. doi:10.1038/nature03702. PMID 15944708.
- ↑ "Specific activation of microRNA-127 with downregulation of the proto-oncogene BCL6 by chromatin-modifying drugs in human cancer cells". Cancer Cell 9 (6): 435–43. June 2006. doi:10.1016/j.ccr.2006.04.020. PMID 16766263.
- ↑ "Specific expression of miR-17-5p and miR-127 in testicular and central nervous system diffuse large B-cell lymphoma". Mod. Pathol. 22 (4): 547–55. April 2009. doi:10.1038/modpathol.2009.10. PMID 19287466.
- ↑ "Down-regulation of the microRNAs miR-34a, miR-127, and miR-200b in rat liver during hepatocarcinogenesis induced by a methyl-deficient diet". Mol. Carcinog. 48 (6): 479–87. June 2009. doi:10.1002/mc.20484. PMID 18942116. https://zenodo.org/record/1229287.
Further reading
- "Specific activation of microRNA-127 with downregulation of the proto-oncogene BCL6 by chromatin-modifying drugs in human cancer cells.". Cancer Cell 9 (6): 435–43. 2006. doi:10.1016/j.ccr.2006.04.020. PMID 16766263.
- "Aberrant epigenetic reprogramming of imprinted microRNA-127 and Rtl1 in cloned mouse embryos.". Biochem Biophys Res Commun 379 (2): 390–4. 2009. doi:10.1016/j.bbrc.2008.12.148. PMID 19126398.
- "Expression Profile of MicroRNAs in Serum: A Fingerprint for Esophageal Squamous Cell Carcinoma.". Clin. Chem. 56 (12): 1871–9. December 2010. doi:10.1373/clinchem.2010.147553. PMID 20943850.
External links
 |  |
