Chapter 16: molecular basis of inheritance Flashcards
Frederick Griffith
studied strains of streptococcus and discovered transformation
- treated mice with pathogenic S strain, nonpathogenic R strain, heat-killed S strain
- found that heat-killed S cells and living R cells killed mice
transformation
change in genotype/phenotype due to assimilation of external DNA by cell
Avery, McCarty, MacLeod
found that transforming agent was DNA
bacteriophages
virus that infects bacteria
virus
DNA enclosed by protective coat (mostly protein)
Hershey & Chase
used radioactive sulfur and phosphorus to trace protein/DNA of T2 phages that infect bacteria. found that phages inject DNA and so DNA carries hereditary material
Chargaff’s rules
- base composition varies between species
- A = T, G = C
double helix
DNA has 2 strands in a helix shape
antiparallel
two sugar-phosphate backbones go in opposite directions
purines
adenine and guanine
pyrimidines
thymine and cytosine
base pairing in DNA
- 2 hydrogen bonds between A and T
- 3 hydrogen bonds between G and C
semiconservative model
each daughter DNA has template parent strand and one newly made strand
conservative model
two parental strands reassociate after acting as templates for new strands
dispersive model
each strand of both daughter molecules has mixture of both parent and newly synthesized DNA
Meselsohn & Stahl
cultured bacteria with heavy isotope 15N (nitrogen) and then transferred to medium with 14N (lighter). centrifuged DNA samples from bacteria to separate DNA of different densities
origins of replication
short stretches of DNA with specific sequences where DNA replication starts
replication fork
region where parental strands of DNA are unwound in a replication bubble (eukaryotes)
helicase
separate DNA at replication forks
single-strand binding proteins
keeps DNA apart in replication
topoisomerase
relieves tension ahead of replication fork in DNA
primer
RNA chain used in initiation of DNA synthesis
DNA polymerases
catalyze synthesis of DNA by adding nucleotides to preexisting chain in 5-3 direction
- adds nucleotriphosphate, which loses 2 phosphate as pyrophosphate
- hydrolysis of pyrophosphate to 2 molecules of inorganic phosphate is coupled exergonic reaction that helps drive polymerization reaction
primase
synthesizes RNA primer
leading strand
strand elongated continuously in 5-3 direction
lagging strand
strand elongated in fragments away from replication fork in 5-3 direction
Okazaki fragments
segments of lagging strand. 1000-2000 bp long in E. coli, 100-200 bp long in eukaryotes
DNA polymerase 3
adds nucleotides
DNA polymerase 1
replaces RNA primer with DNA
DNA ligase
joins sugar-phosphate backbones of Okazaki fragments
mismatch repair
other enzymes remove/replace incorrectly paired nucelotides
nuclease
DNA-cutting enzyme
nucleotide excision repair
nuclease cuts damaged DNA and DNA polymerse/ligase fills in gap
xeroderma pigmentosum
defect in nucleotide excision repair enzyme. sensitive to sunlight (cause UV rays can cause thymine dimers)
telomeres
special nucleotide sequences at the ends of eukaryotic chromosomal DNA molecules that protects it
- not needed in circular prokaryote DNA
telomerase
catalyzes lengthening of telomeres in eukaryotic germ cells
nucleoid
dense region of bacteria in bacterium not membrane-enclosed
chromatin
complex of DNA and protein
histones
proteins involved in DNA packing in chromatin. about 100 amino acids, 1/5 of which are positively charged (to bind to negative DNA).
- H2A, H2G, H3, H4: used in nucleosomes
nucleosome/ 10 nm fiber
basic unit of DNA packing. DNA wound twice around protein core of 2 molecules each of four main histone types.
- N terminus (amino end) of each histone extends outwards (histone tail)
linker DNA
“string” between beads of nucleosomes
30 nm fiber
packing because of interactions between histone tails of nucleosome and linker DNA on nucleosomes on either side.
- prevalent in interphase nucleus
looped domains (300 nm fiber)
30 nm fiber forms loops (looped domains) to chromosome scaffold of proteins, which has some topoisomerase and H1 histones.
metaphase chromosomes
looped domains coil in mitotic chromosome (1400 nm)
heterchromatin
highly condensed interphase chromatin
ucrhomatin
more dispersed chromatin. easily transcribed because DNA is more accessible