Chapter 13: Gene Structure and Expression Flashcards

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1
Q

Polypeptide

A

The linking of appropriate amino acids

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2
Q

Transcription

A

The first step of gene expression, in which a particular segment of DNA is copied into RNA by the enzyme RNA polymerase.

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3
Q

Translation

A

Occurs in the cytosol. Ribosomes read
the nucleotide code
of the mRNA and make a polypeptide by linking together the appropriate amino acids. The ribosome reads the mRNA in three base chunks called codons and translates the code into a protein using specific tRNAs. The Stages are initiation→elongation→termination.

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4
Q

Messenger RNA (mRNA)

A

A mobile copy of a gene made during transcription.

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5
Q

What does the ribosome do?

A

Reads 
the nucleotide code 
of the mRNA and makes a polypeptide by linking together the appropriate amino acids. It reads the mRNA in three base chunks called codons and translates the code into a protein using specific tRNAs.

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6
Q

Genetic Code

A

What is translated by the tRNA.

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7
Q

Codon

A

The 3 base chaunks that the ribosome reads the mRNA in before translating them into a protein using tRNAs.

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8
Q

tRNA

A

The transfer interpeters. They translate a code into a protein.

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9
Q

Start/Initiator codons

A

The first codon of a messenger RNA (mRNA) transcript translated by a ribosome.

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10
Q

Stop (nonsense/termination) codons.

A

The first codon of a messenger RNA (mRNA) transcript translated by a ribosome.

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11
Q

RNA polymerase

A

Opens the DNA double helix and begins to move along the DNA strand, making a mobile copy” of the gene, called an mRNA or messenger-RNA.

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12
Q

Promoter

A

Binds the RNA polymerase and signals the start of the gene.

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13
Q

TATA box

A

A sequence found in the promoter that signals where transcription will start.

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14
Q

Transcription unit

A

Contains the information required to direct translation of the amino acid sequence.

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15
Q

Transcription stop point

A

Marks the ends of he gene and signals the end of transcription.

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16
Q

Transcription factor

A

They recognize the promoter region of the gene and direct the interaction of the RNA polymerase with the DNA strand.

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17
Q

Terminators

A

A stop codon terminates transcription.

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18
Q

Precursor-mRNA (pre-mRNA)

A

An immature single strand of messenger ribonucleic acid (mRNA). Pre-mRNA is synthesized from a DNA template in the cell nucleus by transcription.

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19
Q

5’ cap

A

Required for export of the mRNA from the nucleus and for binding of the mRNA to the ribosome so translation can occur.

20
Q

Polyadenylation

A

The addition of a poly(A) tail to a messenger RNA. The poly(A) tail consists of multiple adenosine monophosphates; in other words, it is a stretch of RNA that has only adenine bases. In eukaryotes, polyadenylation is part of the process that produces mature messenger RNA (mRNA) for translation.

21
Q

Poly(A) tail

A

A stretch of RNA that has only adenine bases.

22
Q

Intron

A

Sequences of DNA that are transcribed but are removed before translation.

23
Q

Exon

A

Expressed sequences which are stuck to ether to give the translatable sequence.

24
Q

mRNA splicing

A

A modification of the nascent pre-messenger RNA (pre-mRNA) transcript in which introns are removed and exons are joined. For nuclear encoded genes, splicing takes place within the nucleus after or concurrently with transcription.

25
Q

Initiation

A

For Translation to begin, the small subunit binds to the

mRNA.

26
Q

Elongation

A

During elongation, a new tRNA enters the A-site. The tRNA will match the codon of the mRNA.

27
Q

Termination

A

Encoded by the genetic code, a stop codon will tell the ribosome when to finish translation of a given polypeptide. Rather than a stop tRNA a release factor will bind in the A-site
of the ribosome.

28
Q

Anticodon

A

The complementary sequence to that of the genetic code.

29
Q

Ribonucleoprotein

A

A nucleoprotein that contains RNA, i.e. it is an association that combines ribonucleic acid and protein together (referred also as protein-RNA complexes).

30
Q

Ribosomal RNA

A

The RNA component of the ribosome, and is essential for protein synthesis in all living organisms.

31
Q

Ribosomal Sites (3)

A
  1. A (aminoacyl) site
  2. P (peptidyl) site
  3. E (exit) site
32
Q

A (aminoacyl) site

A

The binding site for the aminoacyl-tRNA on ribosomes.

33
Q

P (peptidyl) site

A

One of two tRNA binding sites on a ribosome that holds the tRNA that is normally linked to the polypeptide chain.

34
Q

E (exit) site

A

Site on the ribosome through which tRNAs pass after they have donated their amino acid to the growing nascent polypeptide chain.

35
Q

Initiator tRNA

A

A special type of transfer ribonucleic acid (RNA) that initiates protein synthesis by binding to the amino acid methionine and delivering it to the small ribosomal subunit.

36
Q

Ribosome binding site

A

An RNA sequence found in mRNA to which ribosomes can bind and initiate translation.

37
Q

Peptidyl-tRNA

A

Formed in the ribosome, it is the tRNA carrying the growing peptide chain.

38
Q

Peptidyl transferase

A

The primary enzymatic function of the ribosome, which forms peptide bonds between adjacent amino acids using tRNAs during the translation process of protein biosynthesis.

39
Q

Release factor

A

Binds in the A site of the ribosome to stop translation.

40
Q

Polysome

A

A cluster of ribosomes held together by a strand of messenger RNA that each ribosome is translating.

41
Q

Signal Peptide

A

A short peptide present at the N-terminus of the majority of newly synthesized proteins that are destined towards the secretory pathway.

42
Q

Mutation

A

The changing of the structure of a gene, resulting in a variant form that may be transmitted to subsequent generations, caused by the alteration of single base units in DNA, or the deletion, insertion, or rearrangement of larger sections of genes or chromosomes.

43
Q

Base-pair substitution

A

A type of mutation involving replacement or substitution of a single nucleotide base with another in DNA or RNA molecule.

44
Q

Missense mutation

A

When the change of a single base pair causes the substitution of a different amino acid in the resulting protein. This amino acid substitution may have no effect, or it may render the protein nonfunctional.

45
Q

Nonsense mutation

A

A mutation in which a sense codon that corresponds to one of the twenty amino acids specified by the genetic code is changed to a chain-terminating codon.

46
Q

Silent mutation

A

DNA mutations that do not significantly alter the phenotype of the organism in which they occur. Silent mutations can occur in non-coding regions (outside of genes within introns), or they may occur within exons.

47
Q

Frameshift mutation

A

A genetic mutation caused by indels (insertions or deletions) of a number of nucleotides in a DNA sequence that is not divisible by three.