Chapter 16 Flashcards
Who of credited with explaining the structure of the DNA double helix?
Watson and Crick
What is required for DNA replication?
RNA primer
Proteins that are involved in packaging the eukaryotic chromosome into “beads” called __ are __
Nucleosomes; histones
Histones
Proteins that are responsible for the first level of DNA packing in chromatin
Evidence to support that DNA strands run anti parallel to each other includes
Hydrogen bonding interactions
X-Ray measurement data
The nitrogenous bases are on the inside
Chargaff’s rules
The information in DNA is contained in
The sequence of nucleotides along the length of the two strands of the DNA molecule
The role of DNA polymerase in DNA replication is to
Attach free nucleotides to the new DNA strand
Telomeres are
Repeating noncoding sequences at the ends of linear eukaryotic chromosomes
A virus that infects bacteria is called a __, which is made up of the macromolecules __ and __
Bacteriophage
DNA
Protein
DNA polymerase are the enzymes that
Catalyze the addition of nucleotides to a preexisting chain
When __ form after an exposure to ultraviolet (UV) light, a __ can remove the damaged nucleotides and replace them with normal nucleotides
Thymidine dimers
Nucleotide excision repair enzyme
A segment of the strand containing damage is
Cut out (excised) by a DNA-cutting enzyme — a nuclease — and the resulting gap is filled in with nucleotides, using the undamaged strand as a template
Enzymes involved in filling the gap are
DNA polymerase
DNA kinase
Nucleotide excision repair enzyme
DNA repair system
Enzyme
Griffith showed that dead __ cells transform living __ cells into living __ cells
Pathogenic
Nonpathogenic
Pathogenic
The 5’ end of a DNA strand always has a free __ group while the 3’ end always has a free __ group
Phosphate
Hydroxyl
Griffith showed that dead __ cells transform living nonpathogenic cells into __ cells
Pathogenic
Nonpathogenic
DNA replication begins at a site called the origin of replication, forming a bubble, which is followed by a __, where parental strands are unwound by __
Replication forks
Helicases
Replication of a chromosome begins at a site called
Origin of replication
Origins of replication
Short stretches of DNA having a specific sequence of nucleotides
Why were so many of the early experiments on DNA carried out on viruses and bacteria?
They have relatively small genomes
Their chromosomes have a simpler structure
They have short generation times
They can interact with each other
The unwinding of DNA at the replication fork causes twisting and strain in the DNA ahead of the fork, which is revealed by an enzyme called
Topoisomerase
Replication of the lagging strand of DNA is accomplished by repeatedly making __ followed by 1,000-2,000 nucleotide segments called
Short RNA primers
Okazaki fragments
DNA polymerase adds nucleotides to the __ of the leading strands, and to the __ of the lagging strands (Okazaki fragments)
3’ end
3’ end
In DNA, the two purines are __ and the two pyrimidines are __
Adenine and guanine
Cytosine and thymine
The two sugar-phosphate strands that form the rungs of a DNA double helix are joined to each other through __
Hydrogen bonds between nucleotide bases
In DNA replication, the next nucleotide if incorporated into the growing polymer at the __ of the molecule by an enzyme called __
3’ (hydroxyl) end
DNA polymerase
DNA replication is correct
Helicases separate the two strands of the double helix, and DNA polymerase and then construct two new strands using each of the original strands as templates
Evidence to support that DNA strands run anti parallel to each other includes
Nitrogenous bases are on the inside
Chargaff’s rules
Hydrogen bonding interactions
X-ray measurement data
The role of DNA polymerase in DNA replication is to
Attach free nucleotides to the new DNA strand
DNA replication
DNA is copied
Transformation
Change in genotype and phenotype due to the assimilation of external DNA by a cell
Bacteriophages
Bacteria eaters
Virus
Little more than DNA or sometimes RNA enclosed by a protective coat, which is often protein
-to produce more, viruses must infect a cell and take over the cell’s metabolic machinery
DNA composed of
Nitrogen containing base, penthouse sugar (deoxyribose), phosphate group
Base compilation varies
Between species
But A=T and C=G
Antiparallel
The two sugar-phosphate backbones
Subunits run in opposite directions
Origins of replication
Replication of a chromosome begins at particular sites
At the end of a replication bubble is
A replication fork
Y-shaped region where the parental strands of DNA are being unwound
Helicases
Enzymes that untwist the double helix at the replication forks, separating the 2 parental strands and making them available as template strands
Function of helicases
Unwinds parental double helix at replication forks
Function of single-strand binding protein
Binds to and stabilizes single-stranded DNA until it is used as a template
Function of topoisomerase
Relieves overwinding strain ahead of replication forks by breaking, swiveling, and rejoining DNA strands
Function of primase
Synthesizes an RNA primer at 5’ end of leading strand and at 5’ end of each Okazaki fragment of lagging strand
Function of DNA pol III
Using parental DNA as a template, synthesizes new DNA strand by adding nucleotides to an RNA primer of a preexisting DNA strand
Function of DNA pol I
Removes RNA nucleotides of primer from 5’ end and replaces them with DNA nucleotides
Function of DNA ligase
Joins Okazaki fragments of lagging strand; on leading strand, joins 3’ end of DNA that replaces primer to rest of leading strand DNA
After the parental strands separate
Single-strand binding proteins bind to the unpaired DNA strands, keeping them from repairing
Topoimerase helps relieve this strain by breaking, swiveling, and rejoining DNA strands
Unwound parental DNA strands now available to serve as templates for the synthesis of new complementary DNA strands
Primer
RNA chains synthesized by enzyme—primase, which starts a complementary RNA chain from a singe RNA nucleotide, adding more RNA nucleotides 1 at a time, using parental DNA strand as template
Completed primer is
Base-paired to the template strand
New DNA will start from end of DNA primer
DNA polymerase
Enzymes that catalyzes the synthesis of new DNA by adding nucleotides to a preexisting chain
Most require a primer and DNA template strand
Leading strand
Remains in the replication fork on that template strand and continuously adds nucleotides to the new complementary strand as the fork progresses
Lagging strand
Works along the other template strand in the direction away from the replication fork. DNA strand elongating in this direction
Leading strand elongated continuously, and lagging strand
Synthesized discontinuously, as a series of segments
Called Okazaki fragments
Enzyme DNA ligase
Joins the sugar phosphate backbone of all Okazaki fragments into a continuous DNA strand
Upon finding an incorrectly paired nucleotide, the polymerase removes
The nucleotides and resumes synthesis
Mismatch pair
Other enzymes remove and replace incorrectly paired nucleotides that have resulted from replication errors
Nuclease
DNA cutting enzyme, cites out the strand containing damage and resulted gap is then filled with nucleotides, using undamaged strand as a template
Called nucleotide excision repair
Mutations can
Change phenotype
Telomeres
Special nucleotide sequences on the ends of eukaryotic chromosomal DNA
Don’t contain genes
Consists of multiple repetitions of one shirt nucleotide sequence
Don’t prevent erosion of genes near the ends of chromosomes; they postpone it
Become shorter during every round of replication
Telomerase
Catalyzes the lengthening of telomeres in eukaryotic germ cells
Chromatin
Complex of DNA and protein, fits into the nucleus through an elaborate system of packing
Histones
These proteins are responsible for the first level of DNA packing in chromatin
Nucleosome
Basic unit of DNA packing
Heterochromatin
Interphase chromatin, visible as irregular clumps with a light microscope to distinguish it from the less compacted, more dispersed, euchromatin
Can only add to the
3’ end
5’ end
Open phosphate
Grow in 5’->3’ direction
Can have more than one
Replication forks
Single strand binding proteins
Bind to and stabilize single stranded DNA
Helicases
Enzymes that untwist the double helix of the replication forks
Topoisomerase
Corrects “overwinding” ahead of replication forks by breaking, swiveling, and rejoining DNA strands
Replication fork
Y shaped region where new DNA strands are elongating at end of each replication bubble
RNA primer provides
The beginning of a nucleotide
DNA polymerase cannot
Initiate synthesis of a polynucleotide; it can only add nucleotides to an existing 3’ end
Initial nucleotide strand is
A short RNA primer
Primase can
Start an RNA chain from scratch and add RNA nucleotides one at a time using the parental DNA as a template
Can only build on
3’ end
Polymerases catalyze
The elongation of new DNA at a replication fork
Most require a primer and a DNA template strand
Each nucleotide that is added to a growing DNA strand is a
Nucleoside triphosphate
Eukaryotic chromosomal DNA molecules have special nucleotide sequences at their ends called
Telomeres
Don’t prevent the shortening of DNA molecules but they postpone the erosion of genes near the ends of DNA molecules
Bacterial chromosome
Circular DNA, small amount of protein
Eukaryotic chromosomes
Linear DNA, large amount of protein