Cell Biology. Stephen R. Bolsover
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3 3.3 Theme: Structures associated with DNA30 nm solenoidcodoneuchromatingeneheterochromatinnucleoidnucleosomeFrom the above list of structures, select the one described by each of the descriptions below.a highly compacted, darkly staining substance comprising DNA and protein found at the nuclear peripherya mass of DNA and associated proteins lying free in the cytoplasma structure formed when a 146 base‐pair length of DNA winds around a complex of histone proteinsthe form adopted by those parts of chromosomes that are being transcribed into RNA
1 In Medical Relevance 3.2 on page 47 we state that a single base substitution in a codon for glycine could result in the substitution of any one of eight different amino acids at this position. Explain this statement and list the eight amino acids. What other kind of mutation could also arise from a single base substitution in a codon for glycine?
4 DNA AS A DATA STORAGE MEDIUM
The genetic material DNA must be faithfully replicated every time a cell divides to ensure that the information encoded in it is passed unaltered to the daughter cells. DNA molecules have to last a long time compared to RNA and protein. The sugar‐phosphate backbone of DNA is a very stable structure because there are no free hydroxyl groups on the sugar – they are all used up in bonds, either to the base or to phosphate. The bases themselves are protected from chemical attack because they are hidden within the DNA double helix. Nevertheless, chemical changes – mutations – do occur in the DNA molecule and cells have had to evolve mechanisms to ensure that mutation is kept to a minimum. Repair systems are essential for both cell survival and to ensure that the correct DNA sequence is passed on to daughter cells. This chapter describes how new DNA molecules are made during chromosome duplication and how the cell acts to correct base changes in DNA.
During replication the two strands of the double helix unwind. Each then acts as a template for the synthesis of a new strand. This process generates two double‐stranded daughter DNA molecules, each of which is identical to the parent molecule. The base sequences of the new strands are complementary in sequence to the template strands upon which they were built. This means that G, A, T, and C in the old strand cause C, T, A, and G, respectively, to be placed in the new strand.
The DNA Replication Fork
Replication of a new DNA strand starts at specific sequences known as origins of replication. The small circular chromosome of Escherichia coli has only one of these, whereas eukaryotic chromosomes, which are usually linear and much larger, have many. At each origin of replication, the parental strands of DNA untwist to give rise to a structure known as the replication fork (Figure 4.1). This unwinding permits each parental strand to act as a template for the synthesis of a new strand. The structure of the double helix and the nature of DNA replication pose a mechanical problem. How do the two strands unwind and how do they stay unwound so that each can act as a template for a new strand?
The DNA molecule must be opened up before replication can proceed. The helix is a very stable structure, and in a test tube the two strands separate only when the temperature reaches about 90 °C. In the cell, the combined actions of several proteins help to separate the two strands. Much of our knowledge of replication comes from studying E. coli, but similar systems operate in all organisms, bacteria, archaea, and eukaryotes. The proteins E. coli uses to open up the double helix during replication include DnaA, DnaB, DnaC, and single‐stranded DNA‐binding proteins.
DnaA Protein
Several copies of the protein DnaA, which is activated by a molecule of ATP, bind to four sequences of nine base pairs within the E. coli origin of replication (ori C). This causes the two strands to begin to separate (or “melt”) because the hydrogen bonds in DNA are broken near to where the DnaA protein binds. The DNA is now in the open complex formation and has been prepared for the next stage in replication, which is to open up the helix even further.
DnaB and DnaC Proteins
DnaB is a helicase. It moves along a DNA strand, breaking hydrogen bonds, and in the process unwinds the helix (Figure 4.1). Two molecules of DnaB are needed, one for each strand of DNA. One DnaB attaches to one of the template strands and moves in the 5′ to 3′ direction; the second DnaB attaches to the other strand and moves in the 3′ to 5′ direction. The unwinding of the DNA double helix by DnaB is an ATP‐dependent process. DnaB is escorted to the DNA strands by another protein, DnaC. However, having delivered DnaB to its destination, DnaC plays no further role in replication.
Single‐Stranded DNA‐Binding Proteins
As soon as DnaB unwinds the two parental strands, they are engulfed by single‐stranded DNA‐binding proteins. These proteins bind to adjacent groups of 32 nucleotides. DNA covered by single‐stranded DNA‐binding proteins is rigid, without bends or kinks. It is, therefore, an excellent template for DNA synthesis. Single‐stranded binding proteins are sometimes called helix‐destabilizing proteins.
In prokaryotes the synthesis of a new DNA molecule is catalyzed by the enzyme DNA polymerase III. Its substrates are the four deoxyribonucleoside triphosphates, dGTP, dATP, dTTP, and dCTP. DNA polymerase III catalyzes the formation of a phosphodiester bond (Figure 3.3 on page 37) between the 3′ hydroxyl of the sugar residue on the most recently added nucleotide and the 5′ phosphate of the incoming nucleotide. The elongation of the new DNA molecule takes place in the 5′ to 3′ direction (Figure 4.2a). The base sequence of a newly synthesized DNA strand is dictated by the base sequence of its parental strand. If the sequence of the template strand is 3′ CATCGA 5′, then that of the daughter strand is 5′ GTAGCT 3′. In eukaryotes, DNA replication is