Chapter 10 Flashcards

1
Q

Differentiate between “point mutations” and “chromosomal mutations”

A

Point: the change only involves a small portion of DNA Chromosomal: changes involve large segments of DNA

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2
Q

How can the consequences of mutations vary depending on the timing of the mutation? (Germline mutations vs. Somatic mutations)

A

Mutations in gamete before fertilization: all cells will have the mutation and the mutation is passes to the next generation (blue eyes) NO mutation in gamete before fertilization: arise in one cell and its daughter cells, not passed to the next generation (cancer)

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3
Q

What type of mutation results in sickle cell anemia, and why?

A

Germline mutation, because all of the cells have the mutation

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4
Q

Explain how mutations in the following genes can cause a cell to become cancerous: Ras

A

Ras – GTP-binding protein that regulates the sell cycle, GTP hydrolysis INACTUVATED GTP-binding proteins, Mutant Ras that cannot hydrolyze the GTP: ‘Stuck in the ACTIVE form, cell division is out of control. ‘gain of function’ mutation

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5
Q

Explain how mutations in the following genes can cause a cell to become cancerous: p53

A

p53 – Tumor-suppressor, loss of function, cell division is out of control (no ‘breaks’)

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6
Q

What is the difference between a “spontaneous mutation” and an “induced mutation?”

A

Spontaneous mutations are NOT caused by outside influence while induced mutations ARE caused by outside influence.

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7
Q

Chemical & physical mutagens, what are their effects on DNA?

A

Physical mutagens cause the DNA double-strand to break while chemical mutagens (probably:) alters the DNA causing mutations and alterations in the DNA

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8
Q

Number of mutations that occur in one cell on a typical day?

A

About 16000

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9
Q

What are 3 of the main types of RNA made by transcription?

A

mRNA (messenger RNA) RNA that codes for protein, tRNA (treanser RNA) RNA that decodes mRNA at the ribosome, rRNA (ribosomal RNA) protein synthesis factory, each ribosome is made of protein and ribosomal RNA

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10
Q

Necessary components to initiate transcription?

A

DNA template, four RNA bases (CTP + GTP + ATP + TTP = NTP)

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11
Q

Define “promoter.” Where is it?

A

Special DNA sequence, this is where RNAP starts to transcribe; how RNAP ‘knows’ what a gene is and what is not a gene

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12
Q

Describe the mechanism of RNA polymerase (what does it do, specifically?)

A

Writes 5’ > 3’, reads template DNA 3’ > 5’, (just like DNA polymerase

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13
Q

What is a “terminator”?

A

Specific DNA sequence that signifies the ‘end’ of a gene, new DNA is released

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14
Q

Define Intron

A

Intron: INTERVENING region- REMOVED from the RNA during splicing

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15
Q

Define Exon

A

Exon: EXPRESSED region- codes for amino acids, STAYS IN THE RNA after splicing

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16
Q

What do “snRNPs” do & how do they do it? (Fig. 10.6 & 10.9)

A

One binds to each end of the intron – Both come together, intact complex: the SPLICOSOME – Splicosome cuts out the intron by forming an intron loop – Exon are ligated together – Spliced intron is degraded

17
Q

Explain the purposes of a 5’ end cap and a poly A tail

A

Protects RNA from nucleases; ensures that only full-length RNAs are translated