unit 5- molecular genetics (11&13) Flashcards

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1
Q

3 main differences between DNA & RNA

A

DNA- thymine
RNA- uracil

DNA-deoxyribose
RNA- ribose

DNA- double helix
RNA- single twisted strand

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2
Q

4 nitrogenous bases in RNA

A
  • uracil
  • adenine
  • guanine
  • cytosine
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3
Q

What are the complements of nucleic bases in RNA?

A
  • adenine & uracil

- guanine & cytosine

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4
Q

what happens during transcription?

A

DNA is turned into RNA

- mRNA is created (like DNA replication, but with only one strand & with uracil instead of thymine)

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5
Q

Where does transcription occur?

A

In the nucleus

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6
Q

translation

A

changing RNA to amino acids to make proteins

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7
Q

reactants and products of translation

A

reactant- mRNA

product- amino acids (proteins)

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8
Q

where does translation occur

A

in ribosomes which are in the cytoplasm

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9
Q

3 parts of a nucleotide in RNA

A
  • ribose sugar
  • nitrogenous base
  • phosphate
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10
Q

3 types of RNA

A
  • messenger RNA (mRNA)
  • ribosomal RNA (rRNA)
  • transfer RNA (tRNA)
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11
Q

codon

A

in RNA, a three-base “word” that codes for one amino acid

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12
Q

what kind of RNA makes up codons

A

rRNA

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13
Q

3 stop codons

A

UAA-UAG-UGA

to stop the ribosome from continuing the sequence and messing up the protein being made

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14
Q

start codon

A

AUG

used to signal where a new amino acid sequence should start

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15
Q

anticodons

A

a triplet of bases that is complementary to the codon in mRNA

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16
Q

what type of RNA makes up anticodon

A

tRNA

17
Q

what is the purpose of the genetic code table?

A

to “translate” what amino acids that codons code for

18
Q

mRNA

A

messenger RNA

  • the primary sequence of bases after transcription
  • carries the codons out of the nucleus and into the cytoplasm
19
Q

rRNA

A

ribosomal RNA

a type of RNA made up to create the ribosome which is needed to change the mRNA into amino acids

20
Q

tRNA

A

transfer RNA

the anticodon and directs the amino acid to match up with the codons (anticodon and amino acids are connected together)

21
Q

mutation

A

any change in the nucleotide sequence of DNA

22
Q

3 types of mutuations

A
  • substitution
  • deletion
  • insertion
23
Q

substitution (mutation)

A

switching out one base for another

Ex) aCtgtca -> aTtgtca

24
Q

deletion (mutation)

A

taking out a base of the sequence

Ex) aCtgtca -> a_tgtca

25
Q

insertion (mutation)

A

adding in a base into a sequence

Ex) actgtca -> aGctgtca

26
Q

mutagen

A

physical or chemical agent that causes mutations

27
Q

Bacteria

A
  • used to introduce new genes into other organisms (plasmids)
  • mass production of useful genes and proteins
  • make medicine (human benefit)
  • can make a lot very fast (easily accessible
28
Q

Biotechnology

A

The use of organisms to perform practical tasks for humans

29
Q

restriction enzymes

A

enzyme that cuts sugar- phosphate bonds in the DNA backbone at specific points within particular nucleotide sequences in DNA

30
Q

plasmids

A

small, circular DNA molecule found in bacteria that is separate from the bacterial chromosome

31
Q

when are restriction enzymes used?

A

to cut apart foreign DNA to move fragments around

32
Q

Cloning DNA

A

1) restriction enzymes cut plasmids in one place and DNA in many places
2) the DNA fragment “sticky end” comes into the plasmid and connects according to the base pairing
3) DNA ligase joins the pieces- forming a recombinant DNA plasmid
4) bacteria takes in the recombinant plasmid
5) cell division results in many recombinant plasmids`

33
Q

PCR

A

polymerase chain reaction

technique that makes many copies of DNA without using a living organism

34
Q

things needed for PCR

A
  • targeted DNA
  • DNA polymerase
  • primers
  • nucleotides
35
Q

process of PCR

A

put all the ingredients in a test tube, then heat it up to create the designated amount of DNA

36
Q

Gel electrophoresis

A

Techniques for sorting DNA fragments

This creates the DNS fingerprint

37
Q

How does gel electrophoresis work?

A

The DNA is charged slightly negative, so when electricity charges the gel, the DNA fragments move through the gel. The smaller the fragment, the further it goes.

38
Q

DNA fingerprinting

A

The banding pattern produced by gel electrophoresis and restriction fragments

(Everyone has a different DNA fingerprint)