The rule A-T; C-G is a complementary base pair, and is semi-conservative replication. The Hydrogen bonds will always pair in these exact pairs.
watson-base pairing
DNA polymerase is what I think you are referring to. It will join free nucleotides into a strand based off of a model template.
Phophodiester bonds are the one that connect the nucleotides next to each other on the same strand. Weak hydrogen bonds join the two complementary nucleotides and thus the two strands of the DNA together.
DNA polymerase join complementary DNA nucleotides together while DNA ligase joins together the gaps left behind from the okizoki fragments.
1) RNA polymerase finds the promote or "start signal" along the DNA sequence. 2) RNA polymerase unwinds and upzips DNA 3) Then the enzyme adds complimentary RNA nucleotides to one DNA strand 4) This continues until a "top signal" is reached at the end of the gene on DNA 5) mRNA is released and leaves the nucleus 6) DNA zips together and twists
Adeninine - Thiamine and Guanine - Cytosine pairs.
watson-base pairing
Covalent bonds. Hydrogen bonds join together the two nucleic bases on the nucleotides to make the double helix.
DNA polymerase is what I think you are referring to. It will join free nucleotides into a strand based off of a model template.
A-T and G-C
Phophodiester bonds are the one that connect the nucleotides next to each other on the same strand. Weak hydrogen bonds join the two complementary nucleotides and thus the two strands of the DNA together.
That depends on the process. During DNA replication, The nucleotides of the lagging strand (Okazaki fragments) are connected by DNA ligase. In transcription, the nucleotides of RNA are connected by RNA polymerase II.DNA Polymerse
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As many as there are sides on the bases.
A base, a sugar, and a phosphate. I didn't know either but I just looked it up (:
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