Ch 7

Cards (41)

    • Nucleosomes help to supercoil the DNA
    • DNA structure suggested a mechanism for DNA replication
    • DNA polymerases can only add nucleotides to the 3’ end of a primer
    • DNA replication is continuous on the leading strand and discontinuous onthe lagging strand
    • DNA replication is carried out by a complex system of enzymes.
    • Some regions of DNA do not code for proteins but have other important functions
    • Application: Rosalind Franklin’s and Maurice Wilkins’ investigation of DNA structure by X-ray diffraction. (beam of x-rays fired at orderly arranged DNA to get orderly pattern which showed the double helix shape "X")
    • Application: Use of nucleotides containing dideoxyribonucleic acid to stop DNA replication in preparation of samples for base sequencing.
    • Application: Tandem repeats are used in DNA profiling (restriction enzyme could cut on either side of the tandem repeat, see pg 352 tb)
    • Skill: Analysis of results of the Hershey and Chase experiment providing evidence that DNA is the genetic material. - 2x solution of T2 bacteriophage one was 32P(DNA) and other 35S (PROTEIN) -> latch onto E.coli -> only 32P was found in Ecoli showed that DNA was genetic material
  • DNA is negatively charged
  • helicase unwinds DNA
  • DNA primase adds an RNA primer to show DNA polymerase 3 where to go
  • single stranded binding proteins prevent seperated DNA strands from reannealing during replication
    • DNA gyrase reduces the torsional strain created by the unwinding of DNA by helicase (via negative super coiling)
    • DNA polymerase 1 removes the RNA primers from the lagging strand and replaces them with DNA nucleotides
    • DNA ligase joins the Okazaki fragments together to form a continuous strand
    • The regions of DNA that do not code for proteins should be limited to regulators of gene expression, introns, telomeres and genes for tRNAs
    • Transcription occurs in a 5’ to 3’ direction
    • Nucleosomes help to regulate transcription in eukaryotes
    • Eukaryotic cells modify mRNA after transcription
    • Splicing of mRNA increases the number of different proteins an organism can produce
    • Gene expression is regulated by proteins that bind to specific base sequences in DNA. eg repressor proteins
    • The environment of a cell and of an organism has an impact on gene expression.
  • the promotor region is where RNA polymerase binds, it is near a gene to be transcribed
  • direct methylation of DNA tends to inhibit gene expression, the amount of DNA methylation varies during a lifetime and is affected by environmental factors
  • RNA polymerase adds the 5 ́ end of the free RNA nucleotide to the 3' end of the growing mRNA molecule.
    • Initiation of translation involves assembly of the components that carry out the process. initiator tRNA carrying start codon -> small subunit -> big subunit
    • Synthesis of the polypeptide involves a repeated cycle of events
    • Disassembly of the components follows termination of translation
    • Free ribosomes synthesize proteins for use primarily within the cell
    • Bound ribosomes synthesize proteins primarily for secretion or for use in lysosomes
    • Translation can occur immediately after transcription in prokaryotes due to the absence of a nuclear membrane.
    • The SEQUENCE and number of amino acids in the polypeptide is the primary structure.
    • The secondary structure is the formation of alpha helices and beta pleated sheets stabilized by hydrogen bonding.
    • The tertiary structure is the further folding of the polypeptide stabilized by interactions between R groups.
    • The quaternary structure exists in proteins with more than one polypeptide chain.
    • Application: tRNA-activating enzymes illustrate enzyme–substrate specificity and the role of phosphorylation.
    • Polar and non-polar amino acids are relevant to the bonds formed between R groups
  • APE backwards is the tRNA binding sites of the large sub-unit of the ribosome