DNA, RNA, and Protein Conventions Flashcards

1
Q

Equivalent and Antiparallel

A
  • Equivalent - no logical way to distinguish the two strands based on physical properties
  • Antiparallel - the strands have an antiparallel arrangement
    • 5’ - 3’ - strand on top
    • 3’ - 5’
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2
Q

Both Strands Can Contain Genes

A
  • both strands can contain “genes” and be transcribed but in different directions.
  • The top strand is the coding strand for gene 1. The bottom strand is the coding strand for gene 2.
  • Often, when genome sequences are concerned, the sequence of only one strand is given.
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3
Q

The Two-Strand Convention

A
  • The coding strand 5’-3’ on the top

- the template strand 3’-5’ on the bottom.

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4
Q

coding strand

A
  • has the same “sense” (direction and sequence) as the mRNA that it codes for.
    • exception of U in RNA and deoxyT in DNA
  • it is called the sense strand or the gene.
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5
Q

template strand

A
  • the strand that basepairs with the incoming nucleotides that are connected by phosphodiester linkage to form RNA in the process of transcription.
  • it is complementary to the mRNA
  • It is also code the non-coding strand, or the anti-sense strand or non-sense strand.
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6
Q

Transcription/RNA polymerase

A
  • template is read 3’-5’.
  • mRNA is synthesized 5’-3’.
  • Therefore has the same “sense” as the gene or coding strand.
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7
Q

Translation/Ribosomes

A
  • mRNA read 5’-3’
  • protein synthesized N-terminal - C-terminal
  • using these conventions, gene, mRNA, and protein all have the same “sense”
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8
Q

Go from coding strand to mRNA

A
  • without flipping

- just switch T’s to U’s

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9
Q

nucleic acids versus proteins

A
  • nucleic acids have 5’ to 3’ ends

- proteins have amino and carboxy termini

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10
Q

The way usually seen

A

5’ gene or coding strand 3’
3’ template strand 5’
I
transcription V

5’ mRNA 3’
I
V
+H3N Protein COO-

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11
Q

Making cDNA

A
  • sequence of the cDNA same as gene.
  • ALWAYS TALKS ABOUT SEQUENCE OF SECOND STRAND
  • most time cDNA made double stranded so we can easily clone and sequence them
  • reverse transcriptase requires polyDT as a primer
  • RNA sensitive to high pH so remove and degrade with NaOH
  • remove loop with single-stranded nucleotides
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12
Q

capital blue

A

exons translated

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13
Q

capital black

A

exons untranslated

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14
Q

lowercase blue

A

introns.

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