16 How Genes Work Flashcards

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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?

A

AUG

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
Q

Nonsense

A
  • Change in nucleotide sequence that results in an early stop codon
  • leads to mRNA breakdown or a shortened polypeptide, usually deleterious
25
Q

Frameshift

A

Addition or deletion of nucleotide

Reading frame is shifted, altering the meaning of all subsequent codons; almost always deleterious

26
Q

What are the three categories of mutations?

A

1) beneficial (increase fitness)
2) neutral (silent)
3) deleterious (decrease fitness)

Most mutations are neutral or slightly deleterious

27
Q

Polyploidy

A

Is an increase in the number of each type of chromosome (chromosome-level mutation)

28
Q

Aneuploidy

A

Is the addition or deletion of a chromosome (chromosome-level mutation)

29
Q

How does chromosome-level mutations change chromosome composition?

A
  • 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.