Traits/inheritance Flashcards

0
Q

Chromosomes are viewed by karyotyping -

Draw __ml of blood. Add _______ to stimulate mitosis. Incubate at ___*C for __to__ days. Add _____, culture for _______ hours to stop mitosis in metaphase. Transfer cells to tube. Transfer to a tube containing a _________. Centrifuge to concentrate cells. Add low-______ solution to eliminate _______ and swell _______. Put cells onto microscope slide and stain with _______ to produce _______. Examine with microscope. Digitalised chromosome images produced to make karyotype.

A

Chromosomes are viewed by karyotyping -

Draw 10-20ml of blood. Add phytohemagglutinin to stimulate mitosis. Incubate at 37*C for 2 to 3 days. Add colcemid to culture for 1 - 2 hours to stop mitosis in metaphase. Transfer cells to tube. Transfer to a tube containing a fixative. Centrifuge to concentrate cells. Add low-salt solution to eliminate red blood cells and swell lymphocytes. Put cells onto microscope slide and stain with giesma to produce g banding. Examine with microscope. Digitalised chromosome images produced to make karyotype.

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1
Q

How many somatic cells do humans have? How many are autosomal?

A

46 chromosomes
44 autosomes (22 pairs)
2 sex chromosomes (1 pair)

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2
Q

What are the 3 main recognisable chromosome features?

A

Size
Centromere position
Banding patterns

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3
Q

What are the 3 centromere positions?

A

Metacentric
Submetacenteic
Acrocentric

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4
Q

What regions to the sex chromosomes pair at during meiosis?

A

Pseudoautosmal regions at tips of the arms

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5
Q

Little or no crossover at meiosis means that Y chromosomes are passed on intact from ______ to son. This is called _______ inheritance.

A

Father

Holandric

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6
Q

In x linked recessive inheritance…
Carrier females will have ___% sons affected and ____% daughters carriers
All daughters of affected males are ____, all sons are _____

A

50% 50%

Daughters - carriers, sons - unaffected

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7
Q

Why are females genetic mosaics?

A

They have 2 X chromosomes and randomly deactivate one copy of each chromosome in each cell in the early embryo (visible as a Barr body)

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8
Q

Why might a pedigree follow non Mendelian inheritance?

A

Maternal/mitochondrial inheritance
Phenocopies
Incomplete penetrance - genetic environment or imprinting

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9
Q

What is a phenocopy?

A

A trait that is not the true phenotype eg. Dyed hair

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10
Q

What is lyonisation?

A

Dosage compensation

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11
Q

What causes chimeras

A

Started with twins
Early stage fusing of fertilised eggs
Half and half of genetic information

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