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Published byScarlett Melton Modified over 9 years ago
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Chapter 10
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Deoxyribonucleic acid Primary function: To store and transmit the genetic information that tells cells which proteins to make and when to make them. Proteins Form the structural units of cells Help control chemical processes within cells.
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Made up of repeating subunits – nucleotides. Each DNA contains two long chains of nucleotides. DNA nucleotide has three parts: Deoxyribose – sugar molecule Phosphate group Nitrogen-containing base – molecule that contains nitrogen; four different kinds.
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AKA nitrogenous bases Four kinds: 1. adenine (A) 2. guanine (G) 3. cytosine (C) 4. thymine (T) A and T always bond together. C and G always bond together.
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1953: James Watson & Frances Crick suggested model for DNA structure. Proposed that DNA is composed of two nucleotide chains that wrap around each other to form a double spiral Like a spiral staircase. Called this shape the double helix.
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Cytosine and guanine always pair Adenine and thymine always pair These pairs of bases are called complementary base pairs. Base pairs are connected to each other by hydrogen bonds. C and G form 3 hydrogen bonds. A and T form 2 hydrogen bonds.
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The process of copying DNA in a cell – replication. The two nucleotide chains separate by unwinding Each chain is template for new nucleotide chain Enzymes called helicases separate the two chains. Helicases move along the DNA molecule and break the hydrogen bonds between the nitrogenous bases, separating the chains. Then enzymes called DNA polymerases bind to the separated chains of DNA.
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As the polymerases move along the separated chains, new chains of DNA are assembled using nucleotides that are complementary to the existing DNA chains. Complementary nature is as follows: One side of the DNA has A-T-C-C-A-G Compliment would be: T-A-G-G-T-C When replication is finished two new exact copies of the original DNA molecule are produced The cell is ready to undergo cell division.
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DNA replication occurs with a high degree of accuracy. Only about 1 error in every 10,000 paired nucleotides. A change in the nucleotide sequence is called a mutation. Can have serious effects on new cells.
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