Midterm study guide Flashcards

1
Q

What is the one gene hypothesis

A

That one gene makes one protein, its actually that one gene can code for 10 or more proteins

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2
Q

Is gene variation the cause of human variaion?

A

no, there is minimal variation, snips and mutations, it more about expression

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3
Q

percent of genome is for protein

A

4%

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4
Q

percent of genome is retroviral

A

10%

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5
Q

what country/people have the larges genome variability

A

East african San Bushmen

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6
Q

How are Mito dena and Y chromosome DNA used in migration studies

A

the mitochondral ager is compaired with the number of mutations on the Y chromosome. this time fram and direction of migraiton can be determined.

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7
Q

How is nuclear DNA differnt from mitochondral dna

A

Nuclear DNA is diploid, and is the DNA of the nucleus
mtDNA exists in a state of ploidy found in numerous mitochondria organelles with, multiplie mtDNA molecules, comes from mother. … .

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8
Q

What are the three main problems with determining cause vs correlation in genetic disease with studies like the GWAS (SLide 27, lecture 1)

A

Chance
Linkage
stratifiction

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9
Q

What does koko and kitty suggest about human behaviorn

A

that its not human behavior. Every human behavior we have has been demonstrated in some other animal

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10
Q

5 ponts of control of genetic expression

A
Chromatin
transcription
translation
post translation into cytoplasm
post translation modifications
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11
Q

TATA and CCAAT boxes are examples of wht

A

promoters

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12
Q

what is exon shuffling

A

Exon shuffling is a molecular mechanism for the formation of new genes. It is a process through which two or more exons from different genes can be brought together ectopically, or the same exon can be duplicated, to create a new exon-intron structure.

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13
Q

Does the exon or intron remain as a section of the Messenger RNA

A

Exon

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14
Q

What is the role of enhancer

A

increases the likllihoood of transcription by encouraging activators to bind to that specific area of the DNA

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15
Q

what molecular groups most often modify histones

A

Methyl
acetyl
phosphate

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16
Q

which epigenetic marker can attach to DNA directly

A

Acetylation

17
Q

what are DNA marker allels

A

a gene or allel that is associated with a specific chromosome, they can be used to identifiy the chromosome or to identifiy other genes or alleles

18
Q

are DNA maker alles biologically active

A

not necessarly biological active or involved in transcriptions

19
Q

Genotype

A

combination of allells the person has

20
Q

phenotype

A

observable trait that is expression of genotype

21
Q

autosomal dominant

A

One allele is required for expression

autosomal chromosome 1-22

22
Q

autosomal recessive

A

2 allels required for expression

autosomal chromosome 1-22

23
Q

x linked recessive

A

On x chromosome, need both to be expressive in females, only one required in males

24
Q

X linked dominant

A

On x chromosome, only need one to be expressive

25
Q

mitochondrial inheritance

A

on mitochondrial chromosome

26
Q

X linked dominant diseases

A
  • Can’t be transmitted from father to sun because fathers only contribute Y to sons
    X linked disease are 2x more common in females because father can give X to daughter
27
Q

missense

A

single base change that can change codon for one amine acid

28
Q

nonsense mutation

A

base change that results in stop codon.

29
Q

gain of function mutation

A

completley new enzyme produced or the enxyme is over produced

30
Q

loss of function

A

cause vital or protective protein to become non function in the cell, ie loss of tumor supressor