Biology:Drosha

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Short description: Ribonuclease III enzyme
Crystal structure of Drosha and DGCR8, which form the core of the microprocessor complex.
A representation of the 3D structure of the protein myoglobin showing turquoise α-helices.
Generic protein structure example

Drosha is a Class 2 ribonuclease III enzyme[1] that in humans is encoded by the DROSHA (formerly RNASEN) gene.[2][3][4] It is the primary nuclease that executes the initiation step of miRNA processing in the nucleus. It works closely with DGCR8 and in correlation with Dicer. It has been found significant in clinical knowledge for cancer prognosis[5] and HIV-1 replication.[6]

History

Human Drosha was cloned in 2000 when it was identified as a nuclear dsRNA ribonuclease involved in the processing of ribosomal RNA precursors.[7] The other two human enzymes that participate in the processing and activity of miRNA are the Dicer and Argonaute proteins. Recently, proteins like Drosha have been found significant in cancer prognosis[5] and HIV-1 replication.[6]

Function

Members of the ribonuclease III superfamily of double-stranded (ds) RNA-specific endoribonucleases participate in diverse RNA maturation and decay pathways in eukaryotic and prokaryotic cells.[8] The RNase III Drosha is the core nuclease that executes the initiation step of microRNA (miRNA) processing in the nucleus.[4][7]

The microRNAs thus generated are short RNA molecules that regulate a wide variety of other genes by interacting with the RNA-induced silencing complex (RISC) to induce cleavage of complementary messenger RNA (mRNA) as part of the RNA interference pathway. MicroRNA molecules are synthesized as long RNA primary transcripts known as a pri-miRNAs, which are cleaved by Drosha to produce a characteristic stem-loop structure of about 70 base pairs long, known as a pre-miRNA.[7] Pre-miRNAs, when associated with EXP5, are stabilized due to removal of the 5' cap and 3' poly(A) tail.[9] Drosha exists as part of a protein complex called the Microprocessor complex, which also contains the double-stranded RNA binding protein DGCR8 (called Pasha in D. melanogaster and C. elegans).[10] DGCR8 is essential for Drosha activity and is capable of binding single-stranded fragments of the pri-miRNA that are required for proper processing.[11] The Drosha complex also contains several auxiliary factors such as EWSR1, FUS, hnRNPs, p68, and p72.[12]

Both Drosha and DGCR8 are localized to the cell nucleus, where processing of pri-miRNA to pre-miRNA occurs. These two proteins homeostatically control miRNA biogenesis by an auto-feedback loop.[12] A 2nt 3' overhang is generated by Drosha in the nucleus recognized by Dicer in the cytoplasm, which couples the upstream and downstream processing events. Pre-miRNA is then further processed by the RNase Dicer into mature miRNAs in the cell cytoplasm.[7][12] There also exists an isoform of Drosha that does not contain a nuclear localization signal, which results in the generation of c-Drosha.[13][14] This variant has been shown to localize to the cell cytoplasm rather than the nucleus, but the effects on pri-miRNA processing are yet unclear.

Both Drosha and Dicer also participate in the DNA damage response.[15]

Certain miRNAs have been found to deviate from conventional biogenesis pathways and do not necessarily require Drosha or Dicer, which is because they do not require the processing of pri-miRNA to pre-miRNA.[12] Drosha-independent miRNAs derive from mirtrons, which are genes that encode for miRNAs in their introns and make use of splicing to bypass Drosha cleavage. Simtrons are mirtron-like, splicing-independent, and do require Drosha mediated cleavage, although they do not require most proteins in the canonical pathway such as DGCR8 or Dicer.[6]

Clinical significance

Drosha and other miRNA processing enzymes may be important in cancer prognosis.[16] Both Drosha and Dicer can function as master regulators of miRNA processing and have been observed to be down-regulated in some types of breast cancer.[17] The alternative splicing patterns of Drosha in The Cancer Genome Atlas have also indicated that c-drosha appears to be enriched in various types of breast cancer, colon cancer, and esophageal cancer.[14] However, the exact nature of the association between microRNA processing and tumorigenesis is unclear,[18] but its function can be effectively examined by siRNA knockdown based on an independent validation.[19]

Drosha and other miRNA processing enzymes may also be important in HIV-1 replication. miRNAs contribute to the innate antiviral defense. This can be shown by the knockdown of two important miRNA processing proteins, Drosha and Dicer, which leads to a significant enhancement of viral replication in PBMCs from HIV-1-infected patients. Thus, Drosha, in conjunction with Dicer, seem to have a role in controlling HIV-1 replication.[6]

References

  1. ↑ "A novel type of RNase III family proteins in eukaryotes". Gene 245 (1): 213–21. March 2000. doi:10.1016/s0378-1119(99)00571-5. PMID 10713462. 
  2. ↑ "A novel type of RNase III family proteins in eukaryotes". Gene 245 (1): 213–21. March 2000. doi:10.1016/S0378-1119(99)00571-5. PMID 10713462. 
  3. ↑ "Human RNase III is a 160-kDa protein involved in preribosomal RNA processing" (in en). The Journal of Biological Chemistry 275 (47): 36957–65. November 2000. doi:10.1074/jbc.M005494200. PMID 10948199. 
  4. ↑ 4.0 4.1 "Entrez Gene: RNASEN ribonuclease III, nuclear". https://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=29102. 
  5. ↑ 5.0 5.1 Slack FJ, Weidhaas JB (December 2008). "MicroRNA in cancer prognosis". The New England Journal of Medicine. 359 (25): 2720-2.
  6. ↑ 6.0 6.1 6.2 6.3 Swaminathan, G., Navas-Martín, S., & Martín-García, J. (2014). MicroRNAs and HIV-1 infection: antiviral activities and beyond. Journal of molecular biology, 426(6), 1178-1197.
  7. ↑ 7.0 7.1 7.2 7.3 "The nuclear RNase III Drosha initiates microRNA processing". Nature 425 (6956): 415–9. September 2003. doi:10.1038/nature01957. PMID 14508493. Bibcode: 2003Natur.425..415L. 
  8. ↑ "Mouse ribonuclease III. cDNA structure, expression analysis, and chromosomal location". BMC Genomics 3 (1): 26. August 2002. doi:10.1186/1471-2164-3-26. PMID 12191433. 
  9. ↑ Sloan, K. E., Gleizes, P. E., & Bohnsack, M. T. (2016). Nucleocytoplasmic transport of RNAs and RNA–protein complexes. Journal of molecular biology, 428(10), 2040-2059.
  10. ↑ "Processing of primary microRNAs by the Microprocessor complex". Nature 432 (7014): 231–5. November 2004. doi:10.1038/nature03049. PMID 15531879. Bibcode: 2004Natur.432..231D. 
  11. ↑ "Molecular basis for the recognition of primary microRNAs by the Drosha-DGCR8 complex". Cell 125 (5): 887–901. June 2006. doi:10.1016/j.cell.2006.03.043. PMID 16751099. 
  12. ↑ 12.0 12.1 12.2 12.3 Suzuki, H. I., & Miyazono, K. (2011). Emerging complexity of microRNA generation cascades. The Journal of Biochemistry, 149(1), 15-25.
  13. ↑ 14.0 14.1 "Cytoplasmic Drosha activity generated by alternative splicing" (in en). Nucleic Acids Research 44 (21): 10454–10466. July 2016. doi:10.1093/nar/gkw668. PMID 27471035. 
  14. ↑ "Site-specific DICER and DROSHA RNA products control the DNA-damage response". Nature 488 (7410): 231–5. August 2012. doi:10.1038/nature11179. PMID 22722852. Bibcode: 2012Natur.488..231F. 
  15. ↑ "MicroRNA in cancer prognosis". The New England Journal of Medicine 359 (25): 2720–2. December 2008. doi:10.1056/NEJMe0808667. PMID 19092157. 
  16. ↑ "Extensive post-transcriptional regulation of microRNAs and its implications for cancer". Genes & Development 20 (16): 2202–7. August 2006. doi:10.1101/gad.1444406. PMID 16882971. 
  17. ↑ "microRNA involvement in human cancer". Carcinogenesis 33 (6): 1126–33. June 2012. doi:10.1093/carcin/bgs140. PMID 22491715. 
  18. ↑ Munkácsy, Gyöngyi; Sztupinszki, Zsófia; Herman, Péter; Bán, Bence; Pénzváltó, Zsófia; Szarvas, Nóra; Győrffy, Balázs (2016-01-01). "Validation of RNAi Silencing Efficiency Using Gene Array Data shows 18.5% Failure Rate across 429 Independent Experiments" (in en). Molecular Therapy: Nucleic Acids 5 (9): e366. doi:10.1038/mtna.2016.66. ISSN 2162-2531. PMID 27673562. 

Further reading

External links

  • Overview of all the structural information available in the PDB for UniProt: Q9NRR4 (Ribonuclease 3) at the PDBe-KB.



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