AP Bio Midterm Key Terms Ch. 17 Flashcards
(47 cards)
5’ cap
The 5’ end of a pre-mRNA molecule modified by the addition of a cap of guanine nucleotide.
A site
One of a ribosome’s three binding sites for tRNA during translation. The A site holds the tRNA carrying the next amino acid to be added to the polypeptide chain. (A stands for aminoacyl tRNA.)
alternative RNA splicing
A type of regulation at the RNA-processing level in which different mRNA molecules are produced from the same primary transcript, depending on which RNA segments are treated as exons and which as introns.
aminoacyl-tRNA synthetase
An enzyme that joins each amino acid to the correct tRNA.
anticodon
A specialized base triplet at one end of a tRNA molecule that recognizes a particular complementary codon on an mRNA molecule.
base-pair substitution
A type of point mutation; the replacement of one nucleotide and its partner in the complementary DNA strand by another pair of nucleotides.
codon
A three-nucleotide sequence of DNA or mRNA that specifies a particular amino acid or termination signal; the basic unit of the genetic code.
deletion
(1) A deficiency in a chromosome resulting from the loss of a fragment through breakage. (2) A mutational loss of one or more nucleotide pairs from a gene.
domain
(1) A taxonomic category above the kingdom level. The three domains are Archaea, Bacteria, and Eukarya. (2) An independently folding part of a protein.
E site
One of a ribosome’s three binding sites for tRNA during translation. The E site is the place where discharged tRNAs leave the ribosome. (E stands for exit.)
exon
A coding region of a eukaryotic gene. Exons, which are expressed, are separated from each other by introns.
frameshift mutation
A mutation occurring when the number of nucleotides inserted or deleted is not a multiple of three, resulting in the improper grouping of the following nucleotides into codons.
insertion
A mutation involving the addition of one or more nucleotide pairs to a gene.
intron
A noncoding, intervening sequence within a eukaryotic gene.
messenger RNA (mRNA)
A type of RNA, synthesized from DNA, that attaches to ribosomes in the cytoplasm and specifies the primary structure of a protein.
missense mutation
The most common type of mutation, a base-pair substitution in which the new codon makes sense in that it still codes for an amino acid.
mutagen
A chemical or physical agent that interacts with DNA and causes a mutation.
mutation
A rare change in the DNA of a gene, ultimately creating genetic diversity.
nonsense mutation
A mutation that changes an amino acid codon to one of the three stop codons, resulting in a shorter and usually nonfunctional protein.
one gene–one polypeptide hypothesis
The premise that a gene is a segment of DNA that codes for one polypeptide.
P site
One of a ribosome’s three binding sites for tRNA during translation. The P site holds the tRNA carrying the growing polypeptide chain. (P stands for peptidyl tRNA.)
point mutation
A change in a gene at a single nucleotide pair.
poly-A tail
The modified end of the 3’ end of an mRNA molecule consisting of the addition of some 50 to 250 adenine nucleotides.
polyribosome (polysome)
An aggregation of several ribosomes attached to one messenger RNA molecule.