| First Author | Gaidamakov SA | Year | 2005 |
| Journal | Nucleic Acids Res | Volume | 33 |
| Issue | 7 | Pages | 2166-75 |
| PubMed ID | 15831789 | Mgi Jnum | J:99446 |
| Mgi Id | MGI:3582150 | Doi | 10.1093/nar/gki510 |
| Citation | Gaidamakov SA, et al. (2005) Eukaryotic RNases H1 act processively by interactions through the duplex RNA-binding domain. Nucleic Acids Res 33(7):2166-75 |
| abstractText | Ribonucleases H have mostly been implicated in eliminating short RNA primers used for initiation of lagging strand DNA synthesis. Escherichia coli RNase HI cleaves these RNA-DNA hybrids in a distributive manner. We report here that eukaryotic RNases H1 have evolved to be processive enzymes by attaching a duplex RNA-binding domain to the RNase H region. Highly conserved amino acids of the duplex RNA-binding domain are required for processivity and nucleic acid binding, which leads to dimerization of the protein. The need for a processive enzyme underscores the importance in eukaryotic cells of processing long hybrids, most of which remain to be identified. However, long RNA-DNA hybrids formed during immunoglobulin class-switch recombination are potential targets for RNase H1 in the nucleus. In mitochondria, where RNase H1 is essential for DNA formation during embryogenesis, long hybrids may be involved in DNA replication. |
