Genetics Flashcards

(42 cards)

1
Q

DNA

A
  • located in nucleus

- contains genetic information to control organism

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2
Q

RNA

A

-transfer molecule which moves genetic information and aids in protein synthesis

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3
Q

Purine

A

have double ring structure (larger)

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4
Q

pyramidines

A

have a single ring structure (smaller)

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5
Q

nitrogenous base

A

-connected by H-bonds
-DNA strands run antiparalell
thymine
cytosine
guanine
andanine

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6
Q

nucleotide

A

made of sugar, phosphate bond, nitrogenous base

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7
Q

gene

A

a short section of DNA responsible for inheriting a particular characteristic

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8
Q

2 parts of cell division

A

Interphase-prepare for division grow , mitosis

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9
Q

Stages of Mitosis

A

Prophase- chromatin condenses and form visible chromosomes
Metaphase-the chromosomes move to cell equator
Anaphase- centromeres split and sister chromatin are pulled apear to opposite poles of cell
Telaphase-cell wall pinched and cytokineses(division of cytoplasm

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10
Q

function of meiosis

A

reproductive cells called gametes (egg and sperm)

-mitosis happening twice

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11
Q

Gametes

A
  • egg and sperm
  • haploid
  • each egg and sperm contain 22 autosomes and one sex chromosomes
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12
Q

haploid

A

half the number of chromosomes as humans 23

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13
Q

Prophase 1

A

-nuclear membrane and nucleolus disappear and spindle fibers form
-similar chromosomes pair to form homologous chromosomes
TETRAD- made up of 4 chromatids

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14
Q

Metaphase 1

A

Independent Assortment -pairs of homologous chromosomes line up along the equator randomly
this is called synapsis

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15
Q

Anaphase 1

A

homologous chromosomes separate and move to opposite poles

known as disjunction

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16
Q

Telophase 1

A

-spindle fibers disappear
-cytokineses
no DNA replication 2 chromatids exist
-sometimes a short period of interphase

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17
Q

Meiosis 2

A

identical to mitotic cell division

18
Q

End result of meiosis

A

-4 non-identical daughter cells
meiosis 1 has diploid set of 46
meiosis 2 has a haploid set of 23

19
Q

gametogenesis

A

end result in production of gametes

20
Q

spermatogenesis

A

production of sperm male gametes

equal sperm with head and flagellum

21
Q

oogenesis

A

production of female gametes (eggs)

  • a diploid cell enlarges and undergoes meiosis 1 but cytoplasm is not equally divided
  • one cell is viable sex cell called primary oocyte while other 3 are polar bodies.
22
Q

2 ways of genetic variation

A
  1. prophase 1 when tips of non-sister chromatids “cross over” in synapsis and exchange genetic info
  2. metaphase 1 - homologous chromosomes independently assort from tetrads
23
Q

non- disjunction

A

Failure of chromosomes to move to opposite poles in anaphase 1
3 copies of the 21st chromosome
known as down’s syndrome

24
Q

hereditary

A

transmission of characteristics from one generation to the next

25
allele
particular DNA form that appears at eh gene location an inherited characteristic (Aa)
26
homologous chromosomes
pairs of chromosomes that carry corresponding DNA codes one from mother one from father.
27
Test cross
test preformed to distinguish between homozygous and heterozygous genotype because the phenotype is the same.
28
Incomplete dominance
-both alleles contribute to the phenotype of the heterozygous individual the result is blending inheritance -P= WW(white) x RR(red) F1 : WR (pink) F2: 1WW:2WR:1RR
29
Co dominance
two alleles are expressed at the same time | so mixture of two colors
30
multiple alleles
more than 2 possible alleles
31
Blood types and alleles
A : IAIA IAi B: IBIB IBi AB: IAIB O: ii
32
women men
XX XY
33
3 sex linked disorders
1. Colour blindness 2. Hemophilia 3. Muscular dystrophy
34
Blood Tests
- test for rh factor and blood sugar level - if fetus has rh factor different from mother the mother develops antibodies to the fetus - attack red blood cells - results in brain damage, blood disease, stillbirth
35
Ultrasoud
- visualization of the fetus - physical abnormalities - chormosomal abnormalities are detected through karyotyping
36
Aminocentesis
- 15th and 18th week - needle inserted into abomen and withdraws amniotic fluid - cells cultured in lab - karyotyped during metaphase - chromosome abnormalities detected
37
AFT (alpha-fetaprotien)
protien made in unborn babies - test mothers blood - identify twins - abnormal levels signal nureal tube spinal defect
38
Genetic Mutation
an error in the DNA sequence | may be chromosomal level
39
4 types of chromosomal mutations
1. deletion - portion is lost 2. duplication - chromosome portion is added 3. Inversion - a portion is inverted 4. Translocation : a portion is switched with another
40
Gene therapy
correcting a genetic defect by introducing a normal gene into the defective cells
41
Somatic gene therapy
-introduce gene to somatic cells -hope normal protien is expressed correct symptoms of genetic defect -currently in clinical trials
42
Germ- Line Therapy
- introduce new gene to sperm and egg cells - gene will be transmitted to offspring - common with animals not done with humans