Chapter 17: Gene Expression Flashcards

1
Q

A modified form of guanine added onto the 5’ end of a pre-mRNA molecule

A

5’ Cap

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2
Q

An enzyme that joins each amino acid to the appropriate tRNA

A

Aminoacyl‐tRNA Synthetase

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3
Q

A nucleotide triplet at one end of a tRNA molecule that base pairs with a particular complementary codon on an mRNA molecule

A

Anticodon

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4
Q

One of ribosomes 3 binding sites for tRNA during translation. A site holds the tRNA carrying the amino acid to be added to the polypeptide chain (aminoacyl-tRNA)

A

A Site

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5
Q

Nontemplate strand of DNA, which has the same sequence as the mRNA except it has thymine instead of uracil

A

Coding Strand

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6
Q

A 3-nucleotide sequence of DNA or mRNA that specifies a particular amino acid or termination signal; the basic unit of the genetic code

A

Codon

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7
Q

This type of genetic mutation occurs when one or more nucleotide pairs are lost in a gene.

A

Deletion Mutation

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8
Q

A sequence within the primary transcript that remains in the RNA after RNA processing

A

Exon

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9
Q

This type of genetic mutation occurs when nucleotides are inserted in or deleted from a gene and the number inserted or deleted is not a multiple of three, resulting in the improper grouping of the subsequent nucleotides into codons.

A

Frameshift Mutation

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10
Q

This type of genetic mutation occurs when one or more nucleotide pairs are added to a gene.

A

Insertion Mutation

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11
Q

A noncoding, intervening sequence within a primary transcript that is removed from the transcript during RNA processing

A

Intron

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12
Q

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

A

Messenger RNA (mRNA)

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13
Q

This type of genetic mutation occurs when one or more nucleotide pairs are added or lost in a gene, resulting in a different amino acid in the primary sequence.

A

Missense Mutation

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14
Q

A change in the nucleotide sequence of an organism’s DNA or in the DNA or RNA of a virus

A

Mutation

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15
Q

A mutation that changes an amino acid codon to one of the 3 stop codons, resulting in shorter and usually nonfunctional protein

A

Nonsense mutation

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16
Q

A type of point mutation in which one nucleotide in a DNA strand and its partner in the complementary strand are replaced by another pair of nucleotides

A

Nucleotide‐Pair Substitution

17
Q

A change in a single nucleotide

A

Point Mutation

18
Q

A sequence of 50 to 250 adenine nucleotides added onto the 3’ end of a pre-mRNA molecule

A

Poly‐A Tail

19
Q

An initial RNA transcript from DNA, also called pre-mRNA when transcribed from a protein-coding gene

A

Primary Transcript

20
Q

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

A

Promoter

21
Q

One of ribosomes 3 binding sites for tRNA during translation. P site holds the tRNA carrying the growing polypeptide chain (peptidyl-tRNA)

A

P Site

22
Q

On an mRNA, the triplet group of ribonucleotides used by the translation machinery during polypeptide synthesis

A

Reading frame

23
Q

RNA molecules that, together with proteins, make up ribosomes; most abundant type of RNA

A

Ribosomal RNA (rRNA)

24
Q

An enzyme that link ribonucleotides into a growing RNA chain during transcription, based on complementary binding to nucleotides on a DNA template strand

A

RNA Polymerase

25
Q

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

A

RNA Processing

26
Q

Sequence of about 20 amino acids at or near the leading end of a polypeptide that targets it to the endoplasmic reticulum

A

Signal Peptide

27
Q

A protein RNA complex that recognizes a signal peptide as it emerges from a ribosome and helps direct the ribosome to the endoplasmic reticulum by binding to a receptor protein on the ER

A

Signal‐Recognition Particle (SRP)

28
Q

A nucleotide pair substitution that has no observable effect on the phenotype; for example, within a gene, a mutation that results in a codon that codes for the same amino acid

A

Silent Mutation

29
Q

A DNA sequence in eukaryotic promoters crucial in forming the transcription initiation complex

A

TATA Box

30
Q

The DNA strand that provides pattern, or template, for ordering, by complementary base pairing, the sequence of nucleotides in an RNA transcript

A

Template Strand

31
Q

The synthesis of RNA using a DNA template

A

Transcription

32
Q

Regulatory protein that binds to DNA and affects transcription of specific genes

A

Transcription Factor

33
Q

The completed assembly of transcription factors and RNA polymerase bound to a promoter

A

Transcription Initiation Complex

34
Q
A

Transfer RNA (tRNA)

35
Q

The synthesis of a polypeptide using the genetic information encoded in an mRNA molecule. There is a change in language from nucleotides to amino acids (monomers). Site of translation: ribosomes

A

Translation

36
Q

The flexibility in the base-pairing rules in which the nucleotide at the 5’ end of a tRNA anticodon can bond with more than one kind of base in the third position (3’ end) of a codon

A

Wobble