Genetics & Heritability Flashcards

(43 cards)

1
Q

D.O Hebb

A

• Genetic & environmental influences are entangled in complex ways

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2
Q

Behavior Genetics

A

Research to determine the degree of genetic basis for a behavior, trait

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3
Q

Behavioral genomics

A

Research that links behaviors with specific genes

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4
Q

Molecular genetics

A

How genes work with in the cell

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5
Q

What are the two laws of heredity?

A
  1. Shared genes

2. Gene pool

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6
Q

Mechanism of inheritance

A

• Chromosomes are made up of genes which are made up of DNA which is made up of 4 nitrogenous bases (1) guanine, (2) adenine, (3) thymine, (4) cytosine

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7
Q

Chormosomes

A
  • 22 pairs of autosomes (mitosis)

* 1 pair of sex choromosomes (meiosis)

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8
Q

Alleles

A

location of a gene for a particular trait

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9
Q

Monozygotic twins

A
  • one egg
  • one zygote
  • identical genetic make up
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10
Q

Dizygotic twins

A
  • 2 eggs
  • 2 sperms
  • 2 zygote
  • same genetic make up as siblings born seperately
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11
Q

Phenotype

A
  • dominant genes expressed

* recessive gene only expressed when paired with another recessive gene

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12
Q

Genotype

A

•all of a persons genes both recessive & dominant

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13
Q

Mendelian Principles (old)

A
  • Principles of dominance
  • principle of segregation
  • principle of independent assortment
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14
Q

Principle of dominance

A

• dominant & recessive genes

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15
Q

principle of segragation

A

Separated into reproductive cells

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16
Q

Principle of independent assortment

A
  • gene that determines one characteristic is not dependent on a gene for another characteristics
  • ex: all ppl with brown hair are not the same height
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17
Q

Mendelian current principles

A
  • polygenic inheritance
  • pleiotropic effects
  • incomplete dominance
  • codominance
  • genomic imprinting
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18
Q

Polygenic inheritance

A

• MIXTURE of genes that will determine many characteristics

19
Q

Pleiotropic effects

A

• any SINGLE gene can have many different effects

20
Q

Incomplete dominance

A
  • not COMPLETELY dominant or recessive

* ex: sickle cell anemia

21
Q

Codominance

A
  • When BOTH genes are expressed

* ex: AB blood type

22
Q

Genomic imprinting

A

only one gene is expressed & the other is “silent”

23
Q

What is the human genome project?

24
Q

Zygote

A

• fertilized egg that begins to divide into cells that will develop into the embryo

25
Chromosomes
• strands of genes that consitutes our existance
26
What is the human genome project?
• complete mapping and understanding of all the genes of human beings
27
Fragile x-syndrome
* Sex-linked * Most common cause of intellectual disability * 1 gene segment on the X chromosome is repeated 200x rather than 5-40x
28
Hemophilia
* Sex-linked * Mostly males * lack of a specific protein * blood continues to flow
29
Huntington's Disease
*  Autosome-linked disorder * dominant gene disorder *  chromosome 4 * lost of muscle control * detected @ older age
30
Tay Sachs Disease
* Autosome-linked disorder * onset about 8 months * Chromosome 15 *  death usually by age 6 * cell death, brain cells begin to die out *  loose motor skills, seizures, vision & hearing loss, intellectual disabled & paralysis.
31
Sickle Cell Anemia
* Autosome-linked disorders * recessive gene * incomplete dominance (can experience some symptoms) * chromosome 11 * s or c shaped blood cells get clogged in the system *  shortness of breath, severe pain, characteristics similar to a stroke *  less likely to have malaria
32
Cystic Fibrosis
* Chromosome 7 *  Autosomal recessive genetic condition * affect lungs & digestive system *  life expectancy to early/mid-aulthood * defective gene causes the fluids to become thick and sticky. Instead of acting as a lubricant, the secretions plug up tubes, ducts and passageways, especially in the lungs and pancreas.
33
Down-syndrome: trisomy-21
* having 3 "21" chromosomes * Mental & physical defects * life expectancy 60 * 1/1000 * higher risk to other diseases such as Alzheimer's, cardiovascular issues
34
Autosome
• any chromosome that is not a sex chromosome
35
Sex chromosomes
• determining sex of organism
36
What are the ways to detect diseases prenatally?
* Amniocentesis * CVS (chronic villus sampling) * AFP (aplhafetoprotein) * Ultrasound
37
Amniocentesis
* sample amniotic fluid | * screens for abnormality by measuring levels of feto protein & fetal cells as early as 16 wks
38
CVS (Chronic villus sampling)
* detects any chromosomal defects *  collect sample of fetal cells from placenta * early as 9 wks
39
AFP
• measured through a blood test
40
Ultrasound
* sound waves * screens for growth, organ defects, chromosomal abnormalities & neural tube defects * checks if fetus is developing normally
41
Niche picking (scar & mccarthey)
* passive (parents make decision) * evocative ( boys & girls respond diff. to env) * active ( actively engaged in what they want to do, but the gene kind of predetermining what they should do) * ex of active: tall male reared towards playing basketball, but he wants to play an instrument
42
Limit setting (gottesman)
* upper & lower limit (genetic) * reaction rate (env) * ex: genie had the genes to walk & talk, but the env she was in did not allow her to grow.
43
Non-shared enviornment
* Plomins model *  same genes, but env evokes diff response * experience NOT shared w/ other members of the family.