Chapter 15- DNA and the Gene: Synthesis and Repair
During the infection, the exterior protein coat, or capsid, of the virus is left behind on the exterior of the host cell
Each deoxyribonucleotide consists of a deoxyribose sugar, a phosphate group, and a nitrogenous base
Deoxyribonucleotides link together into a polymer when a hydroxyl group on the 3' carbon of one deoxyribose and the phosphate group attached to the 5’ carbon of another deoxyribose are joined by a covalent bond called a phosphodiester linkage, or phosphodiester bond
Watson and Crick realized that these antiparallel strands will twist around each other into a double-stranded spiral-or double helix-and that only certain bases fit together snugly in pairs within the helix by complementary base pairing.
The double-helical DNA molecule is stabilized in two ways:
complementary base pairing
interactions between the stacked base pairs inside the helix.
Alternative hypotheses about DNA replication include:
Semiconservative replication: If the parental strands of DNA separated, each one could then be used as a template for the synthesis of a new daughter strand.
Conservative replication: If the bases of both strands temporarily turned out from the helix, they could serve as a template for the synthesis of an entirely new double helix all at once.
Dispersive replication This proposed that the parental double helix was fragmented into small pieces before replication and then each piece was replicated by either a conservative or semi conservative mechanism.
Like all organisms, bacterial cells copy their entire complement of DNA,their genome, before every cell division.
The initial breakthrough on DNA replication came with discovery of an enzyme called DNA polymerase.
The potential energy of the deoxyribonucleotide monomers is first raised by reactions that add two phosphate groups to form deoxyribonucleoside triphosphates (dNTPs).
Initially, the replication bubble forms at a specific sequence of bases called the origin of replication
A replication fork is the Y-shaped region where the parental DNA double helix is separated into single strands and copied.
Single-strand DNA-binding proteins (SSBPs) attach to the separated strands to prevent them from snapping back into a double helix
A topoisomerase is an enzyme that cuts DNA, allows it to unwind, and rejoins it.
A short strand of RNA called a primer that is base-paired to 1e DNA template
The other strand, appropriately called the lagging strand, or discontinuous strand, must be synthesized in a direction αwαy from the moving replication fork.
These short DNAs, which were attached to RNA primers came to be known as Okazaki fragments
Once the RNA primer is removed and replaced by DNA, an enzyme called DNA ligase catalyzes the formation of a phosphodiester bond between the 3’ and 5’ ends of adjacent Okazaki fragments, closing up the backbone
The proteins and enzymes work together in a large macromolecular machine called the replisome
The region at the end of a eukaryotic chromosome is called a telomere
An enzyme called telomerase replicates telomeric DNA. Telomerase catalyzes the synthesis of DNA using an RNA template that is an integral part of the enzyme.
Any cell not involved in gamete formation is a somatic cell.
The ability of DNA polymerase to recognize and remove an incorrect deoxyribonucleotide is called proofreading.
Mismatch repair is a form of error correction that cleans up errors introduced during DNA synthesis
Mismatch repair is the final layer of error detection and correction for errors introduced during DNA synthesis.
Xeroderma pigmentosum (XP) is a rare autosomal recessive disease in humans.
During the infection, the exterior protein coat, or capsid, of the virus is left behind on the exterior of the host cell
Each deoxyribonucleotide consists of a deoxyribose sugar, a phosphate group, and a nitrogenous base
Deoxyribonucleotides link together into a polymer when a hydroxyl group on the 3' carbon of one deoxyribose and the phosphate group attached to the 5’ carbon of another deoxyribose are joined by a covalent bond called a phosphodiester linkage, or phosphodiester bond
Watson and Crick realized that these antiparallel strands will twist around each other into a double-stranded spiral-or double helix-and that only certain bases fit together snugly in pairs within the helix by complementary base pairing.
The double-helical DNA molecule is stabilized in two ways:
complementary base pairing
interactions between the stacked base pairs inside the helix.
Alternative hypotheses about DNA replication include:
Semiconservative replication: If the parental strands of DNA separated, each one could then be used as a template for the synthesis of a new daughter strand.
Conservative replication: If the bases of both strands temporarily turned out from the helix, they could serve as a template for the synthesis of an entirely new double helix all at once.
Dispersive replication This proposed that the parental double helix was fragmented into small pieces before replication and then each piece was replicated by either a conservative or semi conservative mechanism.
Like all organisms, bacterial cells copy their entire complement of DNA,their genome, before every cell division.
The initial breakthrough on DNA replication came with discovery of an enzyme called DNA polymerase.
The potential energy of the deoxyribonucleotide monomers is first raised by reactions that add two phosphate groups to form deoxyribonucleoside triphosphates (dNTPs).
Initially, the replication bubble forms at a specific sequence of bases called the origin of replication
A replication fork is the Y-shaped region where the parental DNA double helix is separated into single strands and copied.
Single-strand DNA-binding proteins (SSBPs) attach to the separated strands to prevent them from snapping back into a double helix
A topoisomerase is an enzyme that cuts DNA, allows it to unwind, and rejoins it.
A short strand of RNA called a primer that is base-paired to 1e DNA template
The other strand, appropriately called the lagging strand, or discontinuous strand, must be synthesized in a direction αwαy from the moving replication fork.
These short DNAs, which were attached to RNA primers came to be known as Okazaki fragments
Once the RNA primer is removed and replaced by DNA, an enzyme called DNA ligase catalyzes the formation of a phosphodiester bond between the 3’ and 5’ ends of adjacent Okazaki fragments, closing up the backbone
The proteins and enzymes work together in a large macromolecular machine called the replisome
The region at the end of a eukaryotic chromosome is called a telomere
An enzyme called telomerase replicates telomeric DNA. Telomerase catalyzes the synthesis of DNA using an RNA template that is an integral part of the enzyme.
Any cell not involved in gamete formation is a somatic cell.
The ability of DNA polymerase to recognize and remove an incorrect deoxyribonucleotide is called proofreading.
Mismatch repair is a form of error correction that cleans up errors introduced during DNA synthesis
Mismatch repair is the final layer of error detection and correction for errors introduced during DNA synthesis.
Xeroderma pigmentosum (XP) is a rare autosomal recessive disease in humans.