DNA replication 1. start with the enzyme helicase to break the Hydrogen bond of DNA that matched bass line, separated by ATP, which damage this is causing the replication fork.2. There will be a single strand DNA binding protein to help handle. This single line fork area so that I preserve cord.3. the RNA Primase is creating a DNA primer. The airline to start a new airline that is going to happen. DNA polymerase III 4. to add a new line with a length of DNA nucleotide RNA derived from the primer to the 5 '-> 3 '.This is to be found the fit line DNA template. The whole line will no longer be a problem because I can plug in to the 5 '-> 3 ' correctly (master is a 3 '-> 5 '), a new call that leading strand. On the other hand, there is the problem of the whole string lagging strand (of 5 '-> 3 ') and therefore have to use a primer to a wide range of short strings in the default 3 '-> 5 ', it is possible to get a new line (okazaki fragment), thon.5. the RNA primer is removed because it is RNA, not DNA (non-notarized) by DNA polemerase I manage with additional nucleotide to Thom instead.6. for the lagging strand polymerase I, it's filling the remaining gaps, DNA ligase to connect it using ATP to make a long line and thon.
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