Lecture 24: Biotechnology II Flashcards

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1
Q

What is cystic fibrosis?

A

Inability to move mucus out of the lungs

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2
Q

How do you find a gene if
you don’t know what protein
it makes?

A

Map it

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3
Q

Gene Mapping

A

Shows where a gene lies on a chromosome and which chromosome it is from

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4
Q

The cystic fibrosis gene shows simple medelian inheritance?

A

Meaning that it is controlled by a single gene with two alleles (one dominant, one recessive)

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5
Q

How to order genes along the chromosome?

A

Recombination:
A pair of genes with a larger recombination are likely farther apart on the chromosome

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6
Q

First, find which chromosome the gene is on?

A

Chromosome 7

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7
Q

Is there a lot of medelian inheritance in humans?

A

No, the majority of inheritance in humans is continuous variation

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8
Q

Restriction Fragment Length Polymorphisms

A

Segregate in a simple mendelian fashion
-Some people have cut sites other don’t

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9
Q

Polymerase chain reaction

A

A way of taking a tiny piece of DNA and amplifying a tiny piece from that DNA(making many copies)

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10
Q

How does PCR work?

A

Add DNA primers these primers. The add DNA polymerase, polymerase will start transcribing from those primers making piece of DNA. Then you repeat the process now with 4 single strands of DNA. Keep doing this roughly 40 times to amplify the DNA

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11
Q

What does two separate strands after adding BAM indicate?

A

The restriction fragment has been cut
Presence of restriction site

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12
Q

Correlation between cystic fibrosis and whether they cut with specific restrictive enzyme.

A

Means the restrictive enzyme and gene for CF are close together

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13
Q

How are alleles and RFLPs similar?

A

Alleles: Variation in the sequence of a gene
RFLPs: Variation in the sequence of the restriction site

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14
Q

Phenotype substitute for RFLPs?

A

They don’t have phenotypes however if you alter a restriction site, this will alter a restriction fragment length which will give it a new band size on the gel

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15
Q

Where do RFLPs come from?

A

Trial and error, look for changes in whether the DNA cuts or not

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16
Q

What does one band mean?

A

Uncut RFLP, lack of restriction site

17
Q

Normal Lung cells

A

Have cilia that wave back and forth and push mucus up and out of the lungs

18
Q

Cystic Fibrosis Lung Cells

A

Due to the misregulation of the chloride, mucus becomes very thick and cilia are not strong enough to move it around

19
Q

Genetic Screening

A

-Knowing the gene helps us to identify carriers
-Prenatal diagnosis
-Preimplantation diagnosis

20
Q

Is the cystic fibrosis allele beneficial?

A

-Being heterozygous for CF is beneficial for typhoid fever