Ribonukleaza H1, takođe poznata kao RNaza H1, je enzim, koji je kod ljudi kodiran RNASEH1genom.[1][2][3] RNaza H1 je nespecifična endonukleaza koja katalizuje presecanje RNK hidrolitičkim mehanizmom.
↑ten Asbroek AL, van Groenigen M, Jakobs ME, Koevoets C, Janssen B, Baas F (June 2002). „Ribonuclease H1 maps to chromosome 2 and has at least three pseudogene loci in the human genome”. Genomics79 (6): 818–23. DOI:10.1006/geno.2002.6776. PMID12036296.
↑Nowotny M, Gaidamakov SA, Ghirlando R, Cerritelli SM, Crouch RJ, Yang W (October 2007). „Structure of human RNase H1 complexed with an RNA/DNA hybrid: insight into HIV reverse transcription”. Mol. Cell28 (2): 264–76. DOI:10.1016/j.molcel.2007.08.015. PMID17964265.
Lima WF, Wu H, Nichols JG, et al. (2003). „Human RNase H1 uses one tryptophan and two lysines to position the enzyme at the 3'-DNA/5'-RNA terminus of the heteroduplex substrate.”. J. Biol. Chem.278 (50): 49860–7. DOI:10.1074/jbc.M306543200. PMID14506260.
Lima WF, Rose JB, Nichols JG, et al. (2007). „The positional influence of the helical geometry of the heteroduplex substrate on human RNase H1 catalysis.”. Mol. Pharmacol.71 (1): 73–82. DOI:10.1124/mol.106.025429. PMID17028157.
Lima WF, Nichols JG, Wu H, et al. (2004). „Structural requirements at the catalytic site of the heteroduplex substrate for human RNase H1 catalysis.”. J. Biol. Chem.279 (35): 36317–26. DOI:10.1074/jbc.M405035200. PMID15205459.
Otsuki T, Ota T, Nishikawa T, et al. (2005). „Signal sequence and keyword trap in silico for selection of full-length human cDNAs encoding secretion or membrane proteins from oligo-capped cDNA libraries.”. DNA Res.12 (2): 117–26. DOI:10.1093/dnares/12.2.117. PMID16303743.
Wu H, Lima WF, Crooke ST (1999). „Properties of cloned and expressed human RNase H1.”. J. Biol. Chem.274 (40): 28270–8. DOI:10.1074/jbc.274.40.28270. PMID10497183.
Wu H, Lima WF, Zhang H, et al. (2004). „Determination of the role of the human RNase H1 in the pharmacology of DNA-like antisense drugs.”. J. Biol. Chem.279 (17): 17181–9. DOI:10.1074/jbc.M311683200. PMID14960586.
Hillier LW, Graves TA, Fulton RS, et al. (2005). „Generation and annotation of the DNA sequences of human chromosomes 2 and 4.”. Nature434 (7034): 724–31. DOI:10.1038/nature03466. PMID15815621.
Lima WF, Wu H, Nichols JG, et al. (2003). „Human RNase H1 activity is regulated by a unique redox switch formed between adjacent cysteines.”. J. Biol. Chem.278 (17): 14906–12. DOI:10.1074/jbc.M211279200. PMID12473655.
ten Asbroek AL, van Groenigen M, Nooij M, Baas F (2002). „The involvement of human ribonucleases H1 and H2 in the variation of response of cells to antisense phosphorothioate oligonucleotides.”. Eur. J. Biochem.269 (2): 583–92. DOI:10.1046/j.0014-2956.2001.02686.x. PMID11856317.
Ota T, Suzuki Y, Nishikawa T, et al. (2004). „Complete sequencing and characterization of 21,243 full-length human cDNAs.”. Nat. Genet.36 (1): 40–5. DOI:10.1038/ng1285. PMID14702039.
Cerritelli SM, Crouch RJ (1998). „Cloning, expression, and mapping of ribonucleases H of human and mouse related to bacterial RNase HI.”. Genomics53 (3): 300–7. DOI:10.1006/geno.1998.5497. PMID9799596.
Cerritelli SM, Frolova EG, Feng C, et al. (2003). „Failure to produce mitochondrial DNA results in embryonic lethality in Rnaseh1 null mice.”. Mol. Cell11 (3): 807–15. DOI:10.1016/S1097-2765(03)00088-1. PMID12667461.
Lima WF, Rose JB, Nichols JG, et al. (2007). „Human RNase H1 discriminates between subtle variations in the structure of the heteroduplex substrate.”. Mol. Pharmacol.71 (1): 83–91. DOI:10.1124/mol.106.025015. PMID17028158.