Chapter 18 Part II Flashcards

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1
Q

Gene expression can be fine-tuned

A
  • after transcription that enables the cell to rapidly respond to specific cellular needs
  • 2 post-transcription ways and 1 post-translation
    1) Alternative RNA splicing
    2) mRNA degradation or destruction
    3) Translation initiation and post-translation
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2
Q

1) Alternative RNA splicing

A
  • different mRNA molecules are produced from the same primary transcript
  • create RNA variation or different lengths
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3
Q

2) mRNA degradation or destruction

A

in the cytoplasm is an important factor in determining the protein synthesis in a cell
- degrade

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4
Q

3) Translation initiation and post-translation

A

of various types of protein processing are also subject to control

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5
Q

Protein processing after translation

A

including cleavage and the addition of chemical groups, are subject to control

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6
Q

Ubiquitin

A

will tag proteins and target them for destruction

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7
Q

Proteasomes

A

giant protein complexes that bind protein molecules and degrade them

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8
Q

Cancer

A

may result from genetic changes that affect normal genes for cell cycle control and gene regulation systems

i.e. Ras, ERK, ELK-1, p53

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9
Q

Oncogene

A

cancer-causing genes

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10
Q

Proto-oncogenes

A

normal cellular genes that code for proteins that stimulate normal growth and division

i.e. RAS, ERK, ELK-1

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11
Q

Tumor-suppressor genes

A

encode proteins that inhibit abnormal cell division

i.e. p53

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12
Q

DNA change of a proto-oncogene

A

that makes a proto-oncogene excessively active converts it to an oncogene, which may promote excessive cell division and cancer

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13
Q

Conversion of photo-oncogene to an oncogene

A

can lead to abnormal stimulation of the cell cycle by

1) movement of DNA
2) Amplification
3) Point mutations

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14
Q

1) Movement of DNA within the genome

A

if it ends up near an active promoter, transcription may increase

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15
Q

2) Amplification of a proto-oncogene

A

increases the number of copies of the gene

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16
Q

3) Point mutations in the proto-oncogene or its control elements:

A

causes an increase in gene expression

17
Q

Mutations

A

in the res photo-oncogene and p53 tumor-suppressor gene are common in human cancers

18
Q

Mutations in the RAS gene

A

can lead to production of a hyperactive RAS protein and increased cell division