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Ribonuclease H

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Title: Ribonuclease H  
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Ribonuclease H

ribonuclease H
Crystallographic structure of E. coli RNase HI.[1]
EC number
CAS number 9050-76-4
IntEnz IntEnz view
ExPASy NiceZyme view
MetaCyc metabolic pathway
PRIAM profile
PDB structures RCSB PDB PDBe PDBsum
Gene Ontology AmiGO / EGO
retroviral ribonuclease H
EC number
IntEnz IntEnz view
ExPASy NiceZyme view
MetaCyc metabolic pathway
PRIAM profile
PDB structures RCSB PDB PDBe PDBsum

Ribonuclease H (RNase H) is a family of non-bacteria to archaea to eukaryotes.

RNase H’s ribonuclease activity cleaves the 3’-O-P bond of RNA in a DNA/RNA duplex substrate to produce 3’-hydroxyl and 5‘-phosphate terminated products. In DNA replication, RNase H is responsible for removing the RNA primer, allowing completion of the newly synthesized DNA.


  • Structure 1
  • Function 2
  • Mechanism 3
  • Genes 4
  • Role in Disease 5
    • HIV-1 5.1
  • Applications 6
    • DNA Amplification 6.1
    • Nucleic acid identification 6.2
  • References 7
  • External links 8


The 3-D structure of RNase H commonly consists of a 5-stranded β-sheet surrounded by a distribution of α-helices.[2] In some RNase H, such as the one found in HIV-1, the enzyme is missing one of the helices known as the C-helix, a positively charged α-helix whose protrusive shape increases substrate binding capacity.[3] The active site of the enzyme is centered around a conserved DEDD motif (composed of residues: D443, E478, D498, and D549) which performs the hydrolysis of the RNA substrate.[4] A magnesium ion is commonly used as a cofactor during the hydrolysis step.[5] It is also a potential but unconfirmed mechanism in which multiple ions are necessary to perform the hydrolysis.[6] The enzyme also contains a nucleic acid binding cleft about 60 Å in length that can encompass a region of 18 bound RNA/DNA base pairs.


Because RNase H specifically degrades only the RNA in RNA:DNA hybrids, it is commonly used in molecular biology to destroy the RNA template after first-strand complementary DNA (cDNA) synthesis by reverse transcription, as well as in procedures such as nuclease protection assays. RNase H can also be used to degrade specific RNA strands when the cDNA oligonucleotide is hybridized, such as the removal of the polyadenine tail from mRNA hybridized to oligo(dT), or the destruction of a chosen non-coding RNA inside or outside the living cell. To terminate the reaction, a chelator, such as EDTA, is often added to sequester the required metal ions in the reaction mixture.


Proposed HIV-1 RNase H mechanism


The following human genes encode proteins with RNase H activity:

Role in Disease

Mutations in the RNASE2 genes are associated with the rare human genetic disorder known as Aicardi–Goutieres syndrome,[7] which manifests as neurological and dermatological symptoms at an early age.[8]

Retroviral RNase H, a part of the viral reverse transcriptase enzyme, is an important pharmaceutical target, as it is absolutely necessary for the proliferation of retroviruses, such as HIV and murine leukemia virus.[9][10] Inhibitors of this enzyme could therefore provide new drugs against diseases like AIDS. While not an effective treatment option, incorporation of 6-deoxythioguanosine has been shown to inhibit RNase H cleavage of the DNA/RNA complex.[11]


Within human immunodeficiency virus type 1 (HIV-1), RNase H exists as a domain in the heterodimeric HIV-1 reverse transcriptase enzyme.[12] HIV-1 carries out reverse transcription, a process that produces new double-stranded DNA from the viral genome's single-stranded RNA. During DNA synthesis, a DNA/RNA hybrid is formed as a replication intermediate and must be cleaved by RNase H before the process can continue. RNase H performs three types of cleaving actions: non-specific degradation of the (+)-strand RNA genome, specific removal of the (-)-strand tRNA primer, and removal of the (+)-strand purine-rich polypurine tract (PPT) primer.[13] RNase H plays a role in the priming of the (+)-strand, but not in the conventional method of synthesizing a new primer sequence. Rather RNase H creates a "primer" from the PPT that is resistant to RNase H cleavage. By removing all bases but the PPT, the PPT is used as a marker for the end of the U3 region of its long terminal repeat.[14]


DNA Amplification

IDT introduced a method - RNase H-dependent PCR (rhPCR) - to increase specificity on polymerase chain reaction by using RNase H2, where it has low activity at room temperature and optimal activity around 70°C to act as hot start PCR feature, from Pyrococcus abyssi and the blocked primers the contain a single ribonucleotide residue. [15][16] PCR on target amplification can start only when the single ribonucleotide residue in the primers with complementary binding to the target DNA lead to its cleavage for primer activation.

Nucleic acid identification

Nucleic acid identification can be achieved by the recognition and binding of target DNA by the designated RNA probe. The enzyme RNase H can selectively and repeatedly destroy on;y RNA probe from DNA−RNA duplexes for signal amplification to detection limit of femtomole level. [17][18] Sensing technology surface plasmon resonance was used to monitor the specific cleavage of RNA probe for microRNA profiling in influenza diagnosis.[17]


  1. ^ ​; Goedken ER, Marqusee S (December 2001). "Native-state energetics of a thermostabilized variant of ribonuclease HI". J. Mol. Biol. 314 (4): 863–871.  
  2. ^ Schmitt TJ, Clark JE, Knotts TA (December 2009). "Thermal and mechanical multistate folding of ribonuclease H". J Chem Phys 131 (23): 235101.  
  3. ^ Schultz SJ, Champoux JJ (June 2008). "RNase H activity: structure, specificity, and function in reverse transcription". Virus Res. 134 (1–2): 86–103.  
  4. ^ Tadokoro T, Kanaya S (March 2009). "Ribonuclease H: molecular diversities, substrate binding domains, and catalytic mechanism of the prokaryotic enzymes". FEBS J. 276 (6): 1482–1493.  
  5. ^ Davies JF, Hostomska Z, Hostomsky Z, Jordan SR, Matthews DA (April 1991). "Crystal structure of the ribonuclease H domain of HIV-1 reverse transcriptase". Science 252 (5002): 88–95.  
  6. ^ Klumpp K, Hang JQ, Rajendran S, et al. (December 2003). "Two-metal ion mechanism of RNA cleavage by HIV RNase H and mechanism-based design of selective HIV RNase H inhibitors". Nucleic Acids Res. 31 (23): 6852–9.  
  7. ^ Crow, Y. J.; Leitch, A.; Hayward, B. E.; Garner, A.; Parmar, R.; Griffith, E.; Ali, M.; Semple, C.; Aicardi, J.; Babul-Hirji, R.; Baumann, C.; Baxter, P.; Bertini, E.; Chandler, K. E.; Chitayat, D.; Cau, D.; Déry, C.; Fazzi, E.; Goizet, C.; King, M. D.; Klepper, J.; Lacombe, D.; Lanzi, G.; Lyall, H.; Martínez-Frías, M. A. L.; Mathieu, M. L.; McKeown, C.; Monier, A.; Oade, Y.; Quarrell, O. W. (2006). "Mutations in genes encoding ribonuclease H2 subunits cause Aicardi-Goutières syndrome and mimic congenital viral brain infection". Nature Genetics 38 (8): 910–916.  
  8. ^ Orcesi, S; La Piana, R; Fazzi, E (2009). "Aicardi-Goutieres syndrome". British Medical Bulletin 89: 183–201.  
  9. ^ Mizuno M, Yasukawa K, Inouye K (February 2010). "Insight into the mechanism of the stabilization of moloney murine leukaemia virus reverse transcriptase by eliminating RNase H activity". Biosci. Biotechnol. Biochem. 74 (2): 440–2.  
  10. ^ Coté ML, Roth MJ (June 2008). "Murine leukemia virus reverse transcriptase: structural comparison with HIV-1 reverse transcriptase". Virus Res. 134 (1–2): 186–202.  
  11. ^ Krynetskaia NF, Krynetski EY, Evans WE (October 1999). "Human RNase H-mediated RNA cleavage from DNA-RNA duplexes is inhibited by 6-deoxythioguanosine incorporation into DNA". Mol. Pharmacol. 56 (4): 841–8.  
  12. ^
  13. ^ Klarmann GJ, Hawkins ME, Le Grice SF (2002). "Uncovering the complexities of retroviral ribonuclease H reveals its potential as a therapeutic target". AIDS Rev 4 (4): 183–94.  
  14. ^ Beilhartz GL, Götte M (March 2010). "HIV-1 Ribonuclease H: Structure, Catalytic Mechanism and Inhibitors". Viruses 2 (4): 900–926.  
  15. ^
  16. ^ Dobosy JR, Rose SD, Beltz KR, Rupp SM, Powers KM, Behlke MA, Walder JA (2011). "RNase H-dependent PCR (rhPCR): improved specificity and single nucleotide polymorphism detection using blocked cleavable primers". BMC Biotechnol. 11: 80.  
  17. ^ a b Loo JF, Wang SS, Peng F, He JA, He L, Guo YC, Gu DY, Kwok HC, Wu SY, Ho HP, Xie WD, Shao YH, Kong SK (2015). "A non-PCR SPR platform using RNase H to detect MicroRNA 29a-3p from throat swabs of human subjects with influenza A virus H1N1 infection". Analyst 140: 4566-4575.  
  18. ^ Goodrich TT, Lee HJ, Corn RM (2004). "Direct detection of genomic DNA by enzymatically amplified SPR imaging measurements of RNA microarrays". J Am Chem Soc. 126: 4086-4087.  

External links

  • GeneReviews/NCBI/NIH/UW entry on Aicardi-Goutières Syndrome
  • RNase H at the US National Library of Medicine Medical Subject Headings (MeSH)
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