WH meiosis and Genetics Flashcards

(43 cards)

0
Q

Haploid

A

N, one half set of chromosomes

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1
Q

Diploid

A

2N, where cells have 2 full sets of chromosomes

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2
Q

Autosomes

A

Non-sex chromosomes

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3
Q

Sex chromosomes

A

X and Y chromosomes that decide sex

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4
Q

Mono hybrid cross

A

Cross for ONE trait

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5
Q

Dihybrid cross

A

Cross examining two traits

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6
Q

Homologous chromosomes

A

Chromosome pairs that are similiar but not identical. Each carries the same genes in the same order, but the alleles for each trait may not be the same. One chromosome of each homologous pair comes from the mother and one comes from the father.

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7
Q

Meiosis

A

Produces cells with half the number of original chromosomes so that two cells can combine to create offspring with a complete number of chromosomes

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8
Q

Prophase I

A

Chromatin condenses, homologous chromosomes come together and intertwine in synapsis. Each pair contains four chromatids- called a tetrad. Crossing over occurs

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9
Q

Tetrad

A

Pairs of attached homologous chromosomes

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10
Q

Crossing over

A

Chromatids of homologous chromosomes break off and exchange equivalent pieces of DNA

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11
Q

Chiasmata

A

Where chromosomes remain joined after crossing over

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12
Q

Metaphase I

A

Homologous pairs align at equatorial plane and attaches to spindle fibre

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13
Q

Anaphase I

A

Homologous pairs deprecate and are pulled to opposite poles, called disjunction.

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14
Q

Disjunction

A

Separation of homologous chromosomes

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15
Q

Telophase I

A

Mem brain forms around each nucleus. Each chromosome has sister chromosomes joined at centromere. Cell devises into two daughter cells with haploid chromosome number

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16
Q

Prophase II

A

Centrioles move to opposite poles and spindle forms

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17
Q

Metaphase II

A

Chromosomes migrate to opposite poles and the spindle fibre forms, chromosomes are separated into sister chromatids

18
Q

Anaphase II

A

Sister chromatids are pulled to opposite poles by spindle fibers

19
Q

Telophase II

A

A nuclear membrane forms around each haploid nucleus. Cytokinesis occurs and two daughter cells are formed, completing four haploid cells

20
Q

Increasing variation

A

Ways of increasing genetic variation:

  • horizontal transfer: can move genetic material between bacteria.
  • crossing over
  • random assortment
  • random fertilization
21
Q

Law of segregation

A

Two alleles for a heritable character segregate independently during gamete formation and end up in different gametes

22
Q

Law of independent assortment

A

Two or more genes assort independently during gamete formation. Only applies to genes located on different chromosomes

23
Q

Complete dominance

A

Ex: Classic crosses. One trait is completley dominant over another

24
Incomplete dominance
Ex: red and white snapdragons make pink - the phenotype is in between parental varieties
25
Co dominance
both alleles affect phenotype in desperate distinguishable ways
26
Pleiotrophy
Genes with multiple phenotypic effects.
27
Epistasis
Expression of a gene at one locus alters that at a second locus
28
Polygenic inheritance
Inherited charecters that vary in gradients along a continum - there is not one specific determined expression . Caused by two or more genes
29
Multiple alleles
When there's more than 2 different alleles for a possible phenotype
30
Pedigree analysis
A tree diagram that shows traits across generations. Mendelian genetics can be applied to the pedigree to understand trait inheritance
31
Chromosome mutations
Nondisjunction resulting in aneuploidy- too many or too few chromosomes
32
Non disjunction
Mishaps in meiotic spindle chromosome distribution. One gamete received two of the same chromosome the other receives none
33
Aneuploidy
When a gamete has abnormal chromosome number
34
Monosomic
When a gamete has no copy of a particular chromosome it leads to a missing chromosome in the zygote. 2N-1
35
Triatomic
When there is two of one chromosome in a zygote - 2n + 1
36
Polyploidy
When an organism has more than 2 complete sets of chromosomes
37
Gene mapping
Mapping where on each chromosome different genes lie
38
Chromosome breakage
Chromosome structure changes
39
Deletion
When a fragment of a chromosome is lost
40
Duplication
When a deleted fragment becomes attached as an extra segment to a sister chromatid. It can also attach to a non sister chromatid which results in non identical segments
41
Inversion
When a chromosomal fragment reattaches to the original chromosome in reverse orientation
42
Translocation
When a fragment joins a homologous chromosome. Least harmful