Module 3A and some 3B Flashcards

(39 cards)

1
Q

what is coat color determined by

A

two pigments eumalanin (dark) and pheomelanin (light)

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2
Q

syntheis of pigments is controlled by which gene

A

Mc1r gene

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3
Q

wildtype produces which type of melanin more

A

pheomelanin (light)

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4
Q

mutant produces which time of melanin more

A

eumelanin (dark)

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5
Q

where is the receptor of Mc1r gene embedded

A

in the membrane of meloncytes

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6
Q

what is triggered by the bindg of alpha MSH and Mc1r

A

eumelanin

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7
Q

what is produced by the absence of alpha MSH binding

A

phaeomelanin

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8
Q

what are mutations a source of

A

genetic variation

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9
Q

For dark and light pigment phenotypes how do the proteins differ

A

protein for brown pigment: enzyme required for pigment synthesis
protein for no pigment: enzyme required for pigment synthesis does not work

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10
Q

what is a gene

A

nucleotide sequence that codes for the primary strcture of a specific polypeptide

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11
Q

central dogma

A

process in which the genetic information flows from DNA to RNA to make functional product protein

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12
Q

Dogma

A

principles or rules that facilitate phenomenons

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13
Q

proteins _____ traits while DNA _____ proteins

A

produces; encodes

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14
Q

replication

A

synthesis of a new DNA strand

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15
Q

transcription

A

syntheis of RNA using information from DNA; information is transcribed or rewritten from DNA to a complimentary strand of RNA (mRNA)

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16
Q

mRNA

A

carries a genetic message from DNA to the ribosome

17
Q

ribosome

A

protein syntheisizing machinery of the cell

18
Q

translation

A

syntheis of a polypeptide using infor from the mRNA; carried out by ribosome

19
Q

codon

A

mRNA nucleotide triples (UGG - > tryptophan

20
Q

start codon

A

first codon of an mRNA trascript translated by a ribosome

21
Q

mutation

A

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

22
Q

silent mutations

A

have no effect on the amino acid encoded because of the redundancy in the genetic code

23
Q

missense mutations

A

still code for an amino acid, but not the correct amino acid

24
Q

nonsense mutations

A

change in amino acid codon into a stop codon nearly always leading to a nonfunctional protein

25
insertion
adding protein
26
substitution
exhanging proteins
27
deletion
getting rid of protein
28
why do insertions and deletions have a greater effect than substitution
due to downstream consequences
29
transcription and translation are compartmentalized in eukaryotic cells but not in
prokaryotes
30
what represents the first stage of gene expression
transcription
31
RNA polymerase
catalyzes RNA synthesis
32
What is the newly made RNA complementary to
DNA template strand
33
what is stage one of transcription
initiation: RNA polymerase unwinds and initiates RNA synthesis
34
promoter
specific nucleotide sequence of a gene that binds RNA polymerase. helps position the start point of transcription
35
what does a eukaryotic promoter include
TATA box
36
stage 2 of trasncription
Elongation: after RNA polymerase binds to the promoter, it unwinds a short segment of DNA (transcription bubble) and starts forming the RNA transcript
37
what may insertions and deletions lead to
frameshift mutations: lead to nonfunctional proteins unless frameshift is near the end of the gene
38
frameshift mutation
mutation occurring 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
39
stage three of transcription
termination: transcription continues until RNA polymerase reaches a termination signal in the DNA sequence which releases the RNA polymerase and newly synthesized RNA