Chapter 17 Flashcards

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1
Q

The process by which DNA directs the synthesis of proteins or, in some cases, just RNAs.

A

gene expression

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2
Q

The synthesis of RNA using a DNA template

A

transcription

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3
Q

A type of RNA, synthesized using a DNA template that attaches to ribosomes in the cytoplasm and specifies the primary structure of a protein.

A

messenger RNA

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4
Q

The synthesis of a polypeptide using the genetic information encoded in an mRNA molecule. There is a change of “language” from nucleotides to amino acids.

A

translation

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5
Q

A complex of rRNA and protein molecules that functions as a site of protein synthesis in the cytoplasm; consists of a large and a small subunit. In eukaryotic cells, each subunit is assembled in a nucleolus.

A

ribosomes

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6
Q

A set of three-nucleotide-long words that specific the amino acids for polypeptide chains.

A

triplet code

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7
Q

The DNA strand that provides the pattern, or template, for ordering the sequence of nucleotides in an RNA transcript.

A

template strand

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8
Q

An enzyme that links ribonucleotides into a growing RNA chain during transcription.

A

RNA polymerase

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9
Q

A specific nucleotide sequence in DNA that binds RNA polymerase, positioning it to start transcribing RNA at the appropriate place.

A

promoter

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10
Q

In bacteria, a sequence of nucleotides in DNA that marks the end of a gene and signals RNA polymerase to release the newly made RNA molecule and detach from the DNA.

A

terminator

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11
Q

A regulatory protein that binds to DNA and affects transcription of specific genes.

A

transcription factors

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12
Q

Modification of RNA transcripts, including splicing out of introns, joining together of exons and alterations of the 5’ and 3’ ends.

A

RNA processing

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13
Q

A noncoding, intervening sequence within a primary transcript that is removed from the transcript during RNA processing; also refers to the region of DNA from which this sequence was transcribed.

A

introns

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14
Q

A sequence within a primary transcript that remains in the RNA after RNA processing; also refers to the region of DNA from which this sequence was transcribed.

A

exons

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15
Q

A large complex made up of proteins and RNA molecules that splices RNA by interacting with the ends of an RNA intron, releasing the intron and joining the two adjacent exons.

A

spliceosome

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16
Q

A type of eukaryotic gene regulation at the RNA-processing level in which different mRNA molecules are produced form the same primary transcript, depending on which RNA segments are treated as exons and which as introns.

A

alternative RNA splicing

17
Q

A nucleotide triplet at one end of a tRNA molecule that recognizes a particular complementary codon on an mRNA molecule.

A

anticodon

18
Q

Flexibility in the base-pairing rules in which the nucleotide at the 5’ end of a tRNA anticodon can from hydrogen bonds with more than one kind of base in the third position (3’ end) of a codon.

A

wobble

19
Q

The most abundant type of RNA, which together with proteins makes up ribosomes.

A

ribosomal RNA

20
Q

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)

A

A site

21
Q

A group of several ribosomes attached to, and translating, the same messenger RNA molecule.

A

P site

22
Q

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)

A

E site

23
Q

A group of several ribosomes attached to, and translating, the same messenger RNA molecule.

A

polyribosomes

24
Q

A change in the nucleotide sequence of an organism’s DNA, ultimately creating genetic diversity. Mutations also can occur in the DNA or RNA of a virus.

A

mutation

25
Q

A change in a gene at a single nucleotide pair.

A

point mutation

26
Q

A base-pair substitution that results in a codon that codes for a different amino acid.

A

missense mutation

27
Q

A type of point mutation; the replacement of one nucleotide and its partner in the complementary DNA strand by another nucleotides.

A

base-pair substitution

28
Q

A mutation that changes an amino acid codon to one of the three stop codons, resulting in a shorter and usually nonfunctional protein.

A

nonsense mutation

29
Q

A mutation involving the addition of one or more nucleotide pairs to a gene.

A

insertion

30
Q

A mutational loss of one or more nucleotide pairs from a gene.

A

deletion

31
Q

A mutation occurring when the number of nucleotides inserted or deleted is not a multiple of three, resulting in the improper grouping of the subsequent nucleotides into codons.

A

frameshift mutation

32
Q

A chemical or physical agent that interacts with DNA and causes a mutation.

A

mutagen

33
Q

Causes herpes, diabetes, and syphilis.

A