Genes Flashcards

1
Q

What makes you who you are?

A

We all have characteristics and traits based on what we inherited by our parents in our genes. In addition, environment plats a role in our genes as well.

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2
Q

Modifications to Mendelian Genetics

A
  1. Genetic linkage
  2. sex-linked genes
  3. chromosomal alterations
  4. non-traditional patterns of inheritance
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3
Q

Genes

A
  • sequences of nucleotides in DNA

- arranged linearly in chromosomes

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4
Q

Do all genes assort independently?

A
  • Not true for all genes because some genes are inherited together
  • this is because they are linked genes (on the same chromosome)
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5
Q

Linked genes

A

Genes carried on the same chromosome

  • linked during transmission from parent to offspring
  • inherited like single genes
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6
Q

Is there a way t separate two alleles on the same chromosome?

A

Yes. Through recombination (Prophase 1 in meiosis)

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7
Q

Drosophilia melanogaster

A

A fruit fly

  • model organism for animal genetics
  • Morgan-first genetic map
  • used to test linkage and recombination
  • easy, cheap, fast reproduction time, easy to change DNA
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8
Q

Key to crossing over

A

The closer two genes are the more linked they are because there is less change of crossing over between them

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9
Q

Normal alleles

A
  • usually the most common allele
  • designated by the “+” symbol
  • usually dominant
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10
Q

Dihybrid Testcross Ratio

A

1:1:1:1

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11
Q

Recombination Frequency

A

=# of recombinants/ total progeny

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12
Q

Double cross over

A

gene moves during crossover but comes back in a second crossover

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13
Q

Can genes on the same chromosome ever assort independently?

A

Widely separated linked genes often recombine, which makes them appear to assort independently.
50% recombination frequency=independent assortment `

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14
Q

Why is there a 50% max

A

recombination only between 2 of the 4 chromatids so only half of the gametes will have the recombined chromosomes

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15
Q

Autosomes

A

all chromosomes EXCEPT the sex chromosomes

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16
Q

Human X chromosome

A

large (2350 genes)

many x-linked genes are nonsexual traits

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17
Q

Human Y chromosome

A

small (few genes)
very little homology with the X chromosome
contains SRY gene

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18
Q

Sex linkage

A

female need 2 copies of X-linked alleles (homo recessive)

males need 1 copy of X-linked allele

19
Q

X-linked recessive traits more common in males

A

red-green color blindness, homophilia

20
Q

Pedigree chart

A

shows the genotype and phenotype in a family’s past generations
square=male, circle=female,blue=wild type, red=homozygous

21
Q

Dosage compensation

A

in female mammals, inactivation of one X chromosome makes the dosage of X-linked genes the same as males
occurs during embryonic development

22
Q

Barr Body

A

random inactivation of either X chromosome by condensation

  • attached to side of nucleus
  • copied during mitosis but always remains inactive
23
Q

Deletion

A

broken segment lost from chromosome

24
Q

Duplication

A

broken segment inserted into homologous chromosome

25
Translocation
broken segment attached to nonhomologous chromosome
26
Inversion
broken segment re-attached in reversed orientation
27
CML
cancer of white blood cells
28
ABL gene
- next to the BCR gene it becomes overactive - codes for tyrosine kinase - cells grow out of control
29
Gleevac
drug that inhibits tyrosine kinase
30
Nondisjunction
failure of homologous pair separation during meiosis I | increases with womans age
31
Misdivision
failure of chromatid separation during meiosis II
32
Euploids
normal number of chromosomes
33
Aneuploids
extra or missing chromosomes | usually prevent embryo development (except downs)
34
Polyploids
extra sets of chromosomes because the spindle fails during cell division common and helpful in plants
35
Modes of inheritance
1. Autosomal recessive inheritance 2. autosomal dominant inheritance 3. X-linked recessive inheritance 4. Nontraditional patterns of inheritance
36
Autosomal recessive inheritance
males or females carry a recessive allele on an autosome, homo rec. shows trait -eg cystic fibrosis, albinism, sickle cell
37
Autosomal dominant inheritance
dominant gene is carried on an autosome homozygote dominant or hetero show traits e.g. achondroplaia
38
X linked recessive inheritance
recessive allele carried on X chromosome | e.g. color blindness and hemophilia
39
Prenatal diagnosis
cells obtained from: - embryo - amniotic fluid (amniocentensis) - placenta (chorionic villus sampling)
40
Postnatal genetic screening
biochemical and molecular tests
41
Nontraditional patterns of inheritance
cytoplasmic inheritance and genomic imprinting
42
Cytoplasmic inheritance
- genes carried on DNA in mitochondria or chloroplasts | - follows maternal line
43
Genomic imprinting
expression of an allele is determined by the parent that contributed it - other is silenced (imprinted allele) - usually by methylation
44
Igf2
codes for insulin-like growth factor | -paternal copy is active, maternal is imprinted