Lecture 8c: Molecular Biology- Gene Expression Flashcards

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1
Q

Gene expression

A

the flows of genetic information from the genotype to the phenotype
DNA—>RNA—>Protein

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2
Q

transcription

A

is the process by which the information encoded in DNA is made into a complementary RNA.

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3
Q

the Central Dogma is

A

DNA –(Transcription)-> RNA–(Translation)-> Protein

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4
Q

Gene

A

an organized unit of DNA sequences that enables a segment of DNA to be transcribed into RNA and ultimately results in the formation of a function of a functional product

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5
Q

what is a gene composed of?

A

the promoter, the regulatory sequence, the transcribed region and the terminator

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6
Q

promoter

A

the site in the DNA where RNA polymerase binds to begin transcription

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7
Q

regulatory sequences

A

the sites binding to regulatory proteins control whether a gene is turned on or off

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8
Q

Transcribed region

A

a region of a DNA that is transcribed into an RNA molecule

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9
Q

terminator

A

a sequence that causes the RNA strand to be released from the transcription complex

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10
Q

Transcription molecular processes

A

transcription initiation
transcription elongation
transcription termination

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11
Q

exon

A

a coding portion of the gene

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12
Q

intron

A

a non-coding portion of a gene that is excised from the RNA transcript

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13
Q

RNA splicing

A

the removal of introns and joining of exons in eukaryotic RNA, forming an mRNA molecule with a continuous coding sequence

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14
Q

Capping

A

a 7-methylguanosine attached to the mature eukaryotic mRNAs at the 5’ end

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15
Q

tailing

A

a poly A tail is added to the most mature eukaryotic mRNAs at the 3’ end

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16
Q

the genetic code (simple def)

A

Genetic code refers to the instructions contained in a gene that tell a cell how to make a specific protein.

17
Q

mutation

A

a mutation is the permanent alteration of the nucleotide sequence of the genome of an organism (2 common forms)

18
Q

common gene mutations occur in which 2 ways

A
  1. a base substitution
  2. an insertion or deletion
19
Q

Common forms of mutations

A
  • Base-pair substitution
  • Missense mutation
  • Silent mutation
  • Nonsense mutation
  • Frameshift mutation
20
Q

Base-pair Substitution:

A

Also called point mutation- the replacement of one nucleotide and its partner in the complementary DNA strand with another pair of nucleotides

21
Q

Missense mutation

A

A point mutation in which single nucleotide change results in a codon that codes for a different amino acid

22
Q

Silent Mutation

A

A mutation where a change in a DNA codon does not result in a change in amino acid specified by the gene

23
Q

Nonsense mutation

A

a mutation in which a sense codon that corresponds to one of the 20 amino acids specified by the genetic code is changed to a chain-terminating codon

24
Q

Frameshift mutation

A

a mutation caused by insertions or deletions of a number of nucleotides in a DNA sequence that is not divisible by 3

25
Q

The translation process requires

A

-Amino acids (20AA)
- ATP and GTP
- Enzymes and proteins
- RNAs (mRNA, tRNA, rRNA)
- Ribosomes (small and large subunits)

26
Q

Anticodon

A

the 3-nucleotide segment that base-pairs with a codon in mRNA