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26 Cards in this Set
- Front
- Back
DNA
(deoxryibosenucleic acid) |
the molecule of heredity
-allows genetic information to be passed from one generation to the next |
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Genes
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-discrete packets in heritable information
-comprised of DNA -genes are located on specific areas of chromosomes=locus(loci) -geners are directions for protein synthesis |
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Chromosome
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structure made of DNA and protein(histones)
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Uncondensed DNA
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-long, thread-like structure
-DNA usually exists in this form in a cell nucleus |
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Condensed DNA
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-form that DNA takes prior to cell division
-DNA wraps around histones, forming a nucleosome -Nucleosomes are coiled by other proteins (like a slinky) -those coils are wrapped around proteins scaffolding to form a supercoil |
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Frederick Griffith
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1920s: while attempting to make a vaccine for bacterial pneumonia, discovered that genetic information could be transferred from one strain of bacteria to another (transformation)
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Frederick Griffith's experiment
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-used 2 strains of Streotococcus pneumoniae: R strain-harmless to mice; S strain-deadly to mice
-the heat killed S-strain was mixed with the R-strain(living) and injected into mice as a possible vaccine -mice died, Griffith examined the mice -Griffith found live S-strain bacteria, proving that the genetic material from dead S-strain becaterua moved into the live R-strain bacteria |
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Avery, MacLeod, & McCarty
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1940s: discovered that the molecule that changed the S-strain to the R-strain was DNA
-concluded that genes were made of DNA |
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Hershey & Chase
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1950s: proved that DNA, not protein, was the hereditary material
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"Blender Experiment"
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-Hersehy and Chase used:
radioactive S (sulfur)-found in protein, NOT in DNA radioactive P (phosphorus)-found in DNA, NOT in protein -traced where the radioactivity showed up using viruses(bacterophages) that attack bacteria and replicate inside them -radioactivity showed up inside bacteria (DNA) & not on outside of bacteria (protein coating) when using radioactive P *did experiment twie, once w/ S and once w/ P |
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Nucleotides
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-consist of three parts:
1. phosphate group(PO4) 2. sugar group(deoxyribose) 3. nitrogen-containing base: Adamine, Guanine-purines(double rings) Thymine, Cytosine-pyrimidines(single rings) |
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Structure of DNA
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-shaped like a twisted ladder:double helix
-"backbone" or sides of ladder are mad of alternating sugars & phosphates -"rungs' made of complementary base pairs A=T C=G - - '=': Hydrogen bonds |
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X-ray diffraction
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An analytical technique used to identify crystalline solids by measuring the characteristic spaces between layers of atoms or molecules in a crystal
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Replication
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*prior to cell division, DNA must make an exact copy of itself so that each new cell receives the correct genetic info
*occurs in nucleus *requires enzymes |
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DNA helicase
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breaks apart the DNA helix
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DNA polymerase
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moves along a single strand of DNA matching (pairing) a free nucleotide to one on the exposed strand
- base pairing - catalyzes covalent bonds of sugar and phosphate |
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DNA ligase
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joins the small DNA segments together into one long strand
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Replication bubble
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the unwound portion of the two parental DNA strands, separated by DNA helicase, in DNA replication
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Replication forks
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the place where enzymes synthesize two new DNA strands that are complemtary to the two parental strands
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Free nucleotides
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nucleotides that have not been joined together to form a DNA or RNA strand
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Thymine pair
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T=T
are present when there has been damage by UV rays |
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How does a long, thread-like molecule of DNA condense into a chromosome?
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-uncondensed DNA wraps around histones, forming a nucleosome
-nucleosomes are coiled by other proteins (like a slinky) -those coils are wrapped around a protein scaffolding to form a supercoil |
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How did Hershey and Chase prove that DNA, not protein, was the hereditary material?
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By doing the "Blender Experiment"
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How are the component parts of DNA arranged to form a double helix?
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-shaped like a twisted ladder
-"backbone" made of alternating sugars and phosphates -"rungs" made of complementary base pairs |
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What are the steps of DNA replication?
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1. DNA helicase breaks apart the H-bonds between A,T,C,G - forms replication bubble & 2 replication forks
2. DNA polymerase goest to replicatoin fork site, recognizes chemically nucleotide bases, and then apirs it up with a free nucleotide found floating in the nucleus; the polymerase helps build the "backbone" by bonding sugars to PO4; polymerase always moves to "free sugar" end 3. DNA ligase creates 2 long strands of DNA *replication rate is 100-700 nucleotides at the same time |
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How is UV ray damage to DNA repaired in the cell?
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enzyme removes "thymine pair" and replaces it by A=T; DNA ligase reattach to DNA strands
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