16 How Genes Work Flashcards

0
Q

What two scientist proposed: the one gene, one enzyme hypothesis?

A

George beadle and Edward tatum

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1
Q

What is gene expression?

A

-the process of translating the information in DNA into functioning molecules within the cell

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2
Q

What are nonfunctioning alleles called?

A

Knock-out, null, or loss of function alleles

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3
Q

How did two scientist test one gene, one enzyme hypothesis?

A
  • damage a gene by creating a mutant,
  • then observe the resulting effect on the mutants phenotype

Results: inspired hypothesis and proposed that each gene contains information needed to make an enzyme

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4
Q

What two scientist further tested the one gene, one enzyme hypothesis through the cells production of arginine?

A

Srb and Horowitz

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5
Q

What did Srb and Horowitz hypothesized?

A

Different genes lead to the synthesis of each of the three enzymes required to make arginine

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6
Q

How did Srb and Horowitz test their hypothesis?

A
  • used radiation to create thousands of mutant cells
  • performed genetic screening
  • allowing them to select those mutants incapable of producing arginine
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7
Q

What were the results of Srb and Horowitz experiment?

A

Results support the one-gene, one-enzyme hypothesis

  • three distinct mutants were produced
  • each was deficient in one of the three enzymes in the arginine metabolic pathway

Scientist then understood genes code instruction for making proteins

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8
Q

What is the central dogma of molecular biology?

A

Francis crick proposed:

1) DNA is an information storage molecule
2) the sequence of bases in DNA is a kind of code
3) different combinations of bases specify the 20amino acids

  • a particular stretch of DNA (gene) contains the information to specify the amino acid sequence of one protein.
  • the information encoded in the base sequence of DNA is not directly translated into amino acid sequence of protein.
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9
Q

What two scientist proposed RNA molecules act as a link between genes found in the nucleus and protein-manufacturing centers in cytoplasm?

A

François Jacob and Jacques Monod

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10
Q

What is transcription?

A

The process by which the hereditary information in DNA is copied to RNA

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11
Q

What is translation?

A

The process where the order of nucleotide bases is converted to the order of amino acids.

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12
Q

Central dogma

A
  • organism’s genotype: determined by sequence of bases in DNA
  • organism’s phenotype: determined by the product of the proteins it produces
  • alleles of the same gene differ in their DNA sequence
  • proteins produced by different alleles of the same gene frequently differ in amino acid sequence

DNA —> mRNA —> protein

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13
Q

Exceptions to central dogma

A
  • many genes code for RNA molecules that do not function as mRNA and are not translated into protein. (perform other important functions in the cell)
  • sometimes information flows backwards
  • viral genes maybe composed of RNA and use reverse transcriptase, a viral polymerase, to synthesize as DNA version
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14
Q

Who predicted each word in the genetic code contains three bases?

A

George Gamow

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15
Q

What is a codon?

A
  • The group of three bases

- specifies a particular amino acid

16
Q

What two scientist proved the three base codon?

A

Marshall Nirenberg and Philip Leder

17
Q

What is the code of the start codon?

18
Q

What are the codes for the three stop codons?

A

UGA, UAA, UAG

19
Q

What is a mutation?

A
  • Any permanent change in an organism’s DNA
  • A modification in a cells information archive
  • A change in its genotype
  • Able to create new alleles
20
Q

What are the different types of mutations?

A
  • point mutations: results from a single base change
  • chromosome-level mutations: larger scale, often result from the addition or deletion of chromosomes from the individual’s karyotype
21
Q

When does point mutation occur?

A
  • occur when the DNA polymerase inserts the wrong base into the newly synthesized strand of DNA
  • result in change of the DNA base sequence
  • if the DNA polymerase proof reading and mismatch repair system fails
22
Q

What are missense or replacement mutations?

A

Results in changes in the amino acid sequence of the encoded protein

23
Q

Silent mutations

A

Do not change the amino acids sequence of the gene product

24
Nonsense
- Change in nucleotide sequence that results in an early stop codon - leads to mRNA breakdown or a shortened polypeptide, usually deleterious
25
Frameshift
Addition or deletion of nucleotide Reading frame is shifted, altering the meaning of all subsequent codons; almost always deleterious
26
What are the three categories of mutations?
1) beneficial (increase fitness) 2) neutral (silent) 3) deleterious (decrease fitness) Most mutations are neutral or slightly deleterious
27
Polyploidy
Is an increase in the number of each type of chromosome (chromosome-level mutation)
28
Aneuploidy
Is the addition or deletion of a chromosome (chromosome-level mutation)
29
How does chromosome-level mutations change chromosome composition?
- Inversion: occur when sections of a chromosome break and rotate before rejoining - translocation: occurs when a broken section of one chromosome becomes attached to another.