Module 3A and some 3B Flashcards

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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
Q

insertion

A

adding protein

26
Q

substitution

A

exhanging proteins

27
Q

deletion

A

getting rid of protein

28
Q

why do insertions and deletions have a greater effect than substitution

A

due to downstream consequences

29
Q

transcription and translation are compartmentalized in eukaryotic cells but not in

A

prokaryotes

30
Q

what represents the first stage of gene expression

A

transcription

31
Q

RNA polymerase

A

catalyzes RNA synthesis

32
Q

What is the newly made RNA complementary to

A

DNA template strand

33
Q

what is stage one of transcription

A

initiation: RNA polymerase unwinds and initiates RNA synthesis

34
Q

promoter

A

specific nucleotide sequence of a gene that binds RNA polymerase. helps position the start point of transcription

35
Q

what does a eukaryotic promoter include

A

TATA box

36
Q

stage 2 of trasncription

A

Elongation: after RNA polymerase binds to the promoter, it unwinds a short segment of DNA (transcription bubble) and starts forming the RNA transcript

37
Q

what may insertions and deletions lead to

A

frameshift mutations: lead to nonfunctional proteins unless frameshift is near the end of the gene

38
Q

frameshift mutation

A

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
Q

stage three of transcription

A

termination: transcription continues until RNA polymerase reaches a termination signal in the DNA sequence which releases the RNA polymerase and newly synthesized RNA