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68 Cards in this Set
- Front
- Back
Bacteriophages |
Viruses that infect bacteria |
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Chargaff's Rules |
~the base composition of DNA varies between species ~in all species the number and A and T are equal as are the number of G and C |
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Antiparallel |
containing subunits that run in opposite directions |
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Semiconservative Model of Replication |
predicts that when a double helix replicates, each daughter molecule will have one old strand and one newly made strand |
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Origins of Replication |
where the two DNA strands are separated, opening up a replication "bubble" |
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Replication Fork |
a Y-shaped region where DNA strands are elongating |
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Helicases |
enzymes that untwist the double helix at replication forks |
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Topoisomerase |
corrects "overwinding" ahead of the replication forks by breaking, swiveling, and rejoining DNA strands |
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Primase |
can start an RNA chain and adds RNA nucleotides one at a time using the parental DNA as a template |
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DNA Polymerase |
an enzyme that catalyzes the elongation of new DNA at the replication fork |
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Leading Strand |
strand where DNA polymerase synthesizes continuously, moving toward the replication fork |
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Lagging Strand |
DNA polymerase works in a direction away from the replication fork |
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Okazaki Fragments |
the series of segments synthesized on the lagging strand which are later joined by DNA ligase |
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What direction does DNA synthesize in? |
5' to 3', where the origin of replication is at the 3' end |
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Mismatch Repair |
repair enzymes correct the errors in base pairing |
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Nucleotide Excision Repair |
where a nuclease cuts out the replaces damaged stretches of DNA |
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Telomeres |
special nucleotide sequences at the end of DNA molecules that postpone the erosion of genes near the ends of DNA molecules |
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Telomerase |
an enzyme that catalyzes the lengthening of telomeres in germ cells |
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Nucleoid |
in bacteria, the region of the cell where supercoiled DNA is found |
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Chromatin |
a complex of DNA and protein that is found in the nucleus of most eukaryotic cells |
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Nucleosome |
a structural unit of a eukaryotic chromosome, consisting of a length of DNA coiled around a core of histones |
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Euchromatin |
loosely packed chromatin |
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Heterochromatin |
highly condensed regions of chromatin; typically happens during interphase |
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Gene Expression |
the process by which DNA directs protein synthesis and includes transcription and translation |
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Transcription |
synthesis of a polypeptide using information in the mRNA |
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Ribosomes |
the sties of translation |
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Messenger RNA |
(mRNA) the product of transcription |
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Central Dogma |
The concept that cells are governed by a cellular chain of command: DNA --> RNA --> Protein |
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Triplet Code |
a series of nonoverlapping, three-nucleotide words |
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Template Strand |
one of the two DNA strands that provides a template for ordering the sequence of complementary nucleotides in an RNA transcript |
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Codons |
mRNA base triplets that are read in the 5` to 3` direction that specify one of 20 amino acids to be arranged in a polypeptide |
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Reading Frame |
correct groupings that codons must be read in order for the correct polypeptide to be produced |
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RNA polymerase |
catalyzes RNA synthesis by prying apart DNA strands and hooking together RNA nucleotides |
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Promoter |
the DNA sequence where RNA polymerase attaches |
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Terminator |
the sequence that signals the end of transcription |
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Transcription Unit |
the stretch of DNA that is transcribed |
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3 Stages of RNA Transcription |
~Initiation ~Elongation ~Termination |
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Transcription Factors |
mediate the binding of RNA polymerase and the initiation of transcription |
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Transcription Initiation Complex |
the completed assembly of transcription factors and RNA polymerase II bound to a promoter |
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TATA Box |
a promoter that is crucial in forming the initiation complex in eukaryotes |
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RNA Processing |
the modifying of pre-mRNA by enzymes before the genetic messages are dispatched to the cytoplasm |
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Introns |
noncoding regions of RNA |
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Exons |
regions of RNA that are expressed and usually translated into amino acid sequences |
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RNA splicing |
removes introns and joins exons, creating mRNA molecule with a continuous coding sequence |
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Spliceosomes |
a variety of proteins and several small nuclear ribonucleoproteins (snRNPs) that recognize the splice sites |
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Ribozymes |
catalytic RNA molecules that function as enzymes and can splice RNA |
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Alternative RNA splicing |
some genes can encode more than one kind of polypeptide depending on which segments are treated as exons during splicing |
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Domains |
a modular architecture often had by proteins consisting of discrete regions |
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tRNA |
transfer amino acids to the growing polypeptide chain in a ribosome |
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Wobble |
flexible pairing at the third base of a codon that allows some tRNAs to bind to more than one codon
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Ribosomal RNA |
is the RNA component of the ribosome and is essential for protein synthesis |
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P site |
holds the tRNA that carries the growing polypeptide chain |
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A SIte |
holds the tRNA that carries the next amino acid to be added to the chain |
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E site |
the exit site where discharged tRNAs leave the ribosome |
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3 Stages of Translation |
~Initiation ~Elongation ~Termination |
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Polyribosome |
formed after a number of ribosomes translate a single mRNA simultaneously |
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Free Ribosomes |
synthesize proteins that function in the cytosol |
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Bound Ribosomes |
make proteins of the endomembrane system and proteins that are secreted from the cell |
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Signal Peptide |
what polypeptides destined for the ER or for secretion are marked by |
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Mutations |
changes in the genetic material of a cell or virus |
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Point Mutations |
chemical changes in just one base pair of a gene |
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Mutagens |
physical or chemical agents that can cause mutation |
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Nucleotide-Pair Substitution |
replaces one nucleotide and its partner with another pair of nucleotides |
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Silent Mutations |
have no effect on the amino acid produced by a codon because of redundancy in the genetic code |
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Missense Mutation |
still codes for an amino acid, but not the correct one |
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Nonsense Mutations |
change an amino acid codon into a stop codon, nearly always leading to a nonfunctional protein |
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Insertions and Deletions |
additions or losses of nucleotide pairs in a gene |
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Frameshift Mutation |
an insertion of deletion of nucleotides that alter the reading frame |