M3 Flashcards

1
Q

what are those in common called

A

conserved

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2
Q

what is it called when you compare sequences of genome

A

alligning

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3
Q

what underpins everything about genomes

A

comparing genomes - aligning

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4
Q

when comparing genome within species what are 3 differences that they could be associated

A
  1. diseases
  2. evolutionary history
  3. characteristics
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5
Q

what can we learn if comparing genome between species

A
  1. What sort of genes they have
  2. How differences between species arise
  3. Relationships
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6
Q

T/f DNA bases can be modified when degrade - can sometimes change the sequence

A

true

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7
Q

what 5 things did hey find when looking in a cave for genome

A
  • 4 billion neanderthal nucleotides
    • Develop tools to see if modern
    • Sequence of 3 individuals ( however 2 of them maybe closely relative
    • Enough sequence to compare with modern human genome
      Identified bits of DNA that differ between Neanderthals and us
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8
Q

Modern humans from Europe and Asia carry neanderthal alleles what content doesn’t

A

africa

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9
Q

what type of DNA adds to the varient in our genome that might be related to our phenotype

A

Neanderthals

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10
Q

what are mutation called that are inherited

A

germline

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11
Q

what type of effect does majority of mutations have

A

no effect

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12
Q

what can the outcome of mutations depend on

A
  1. environment
  2. genetic background
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13
Q

t/f In a single gene mutations can have different effects

A

true

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14
Q

t/f Molecule basis in mutation often consistent

A

false - not constant

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15
Q

t/f humans have 2 copies of each gene

A

true
because they are diploid

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16
Q

between dominant and recessive mutation what one occurs when heterozygous

A

dominant

17
Q

explain loss of function
is this recessive or dominant

A

when a gene has a function and it no longer works (broken)
recessive

18
Q

explain gain of function
is this recessive or dominant

A

when a gene works too well or does something unexpected
dominant

19
Q

what does it mean by sex linked

A
  • females are carriers
  • males mostly affected
20
Q

if the trait isn’t seen in every generation of the affected family, passed on by 2 asymptomatic carriers, males and females are equally likely to inherit

A

Autosomal recessive

21
Q

if the affected individual has affected parent, males and females are equally likely to inherit

A

autosomal dominant

22
Q

if the trait is not passed on by males to their sons, most affected is male

A

X-linked recessive

23
Q

If a rare disease is autosomal dominant, what is the probability of a grandchild inheriting disease from an affected grandparent?

A

0.25

24
Q

are adult and embryonic stem cells both pluripotent

A

yes

25
Q

what are the two main function of the genome project

A
  1. identify all human genes and there roles
  2. analysis genetic variation between species