DNA, protein synthesis (topic 1 + 4) Flashcards

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1
Q

structure of the monomer which is called nucleotide

A

a pentose
nitrogen-containing organic base A,C,G,T,U
a phosphate group

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2
Q

nucleotides joining to each other

A

weak hydrogen bonds are easily broken, allowing the strands to separate during replication and protein synthesis

(between complimentary bases)

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3
Q

how are nucleotides joined

A

bond between phosphate group of one, and sugar of other
PHOSPHODIESTER BOND

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4
Q

hydrogen bonds between nitrogen containing bases

A

2 between adenine and thymine
3 between cytosine and guanine

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5
Q

how are nucleotides joined

A

condensation reaction
PHOSPHODIESTER bond, between phosphate group of one, and sugar of other

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6
Q

RNA

A

single stranded and relatively short
pentose sugar = ribose
organic bases = AU, CG

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7
Q

DNA replication process (semi-conservative replication)

A
  • enzyme DNA helicase breaks hydrogen bonds between complementary bases
  • the DNA molecule unwinds and separates into 2 strands
  • both polynucleotide chains act as templates which free nucleotides attach to by complementary base pairs
  • DNA polymerase joins adjacent nucleotides in a condensation reaction (forms phosphodiester bonds)
  • forms 2 new strands of DNA (genetically identical to original strand) (each contain one original strand, one new strand)
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8
Q

what is a gene

A

a section of DNA containing coded information for making polypeptides and functional RNA

enzymes are proteins - due to controlling chemical reactions they are responsible for an organisms development and activities, so along with environmental factors, genes determine the nature and development of all organisms

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9
Q

where are genes located

A

a locus (on a DNA molecule)

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10
Q

genetic code (movement in terms of basic protein synthesis)

A

always remains safe inside the nucleus
- proteins are made outside the nucleus in the cytoplasm so a copy of the genetic code of a gene is made
this copy passes out of the nucleus into the cytoplasm

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11
Q

what is a triplet

A

3 DNA bases that code for a specific amino acid

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12
Q

degenerate code and stop code

A

d: most amino acids are coded for by more than one triplet

s: triplets that code for a stop (marks the end of the polypeptide chain)

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13
Q

what are exons and introns

A

exons: sequences that code for amino acids
introns: non-coding sequences that separate exons in a gene

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14
Q

genetic code is universal and non-overlapping

A

universal: triplets that code for an amino acid are the same in almost all organisms (indirect evidence to evolution)

non-overlapping: each base in a sequence is read only one eg 123 456

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15
Q

differences in DNA between prokaryotic and eukaryotic cells

A

pro: DNA molecules are shorter, not associated with protein molecules, circular DNA, don’t form chromosomes, found in cytoplasm

eu: dna molecules are longer, associated with histones, linear DNA, form chromosomes, found in nucleus (but also in mitochondria and chloroplasts - dna there is like prokaryotic)

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16
Q

chromosomes visibility

A

only visible as distinct structures when a cell is dividing, rest of the time chromatin is widely dispersed throughout the nucleus

17
Q

chromosome structure

A

one chromosome = two chromatids (because dna has already replicated to give 2 identical dna molecules) joined at a point called the centromere

DNA is highly coiled and held by histones so 2m of dna can be stored in every human cell

18
Q

homologous chromosomes

A

2 chromosomes that contain the same genes (but not necessarily the same alleles) pair up - look like this ))((

19
Q

allele

A

different forms of the same gene

20
Q

diagram structure of mRNA and tRNA

A

mRNA = ribose and phosphate backbone, A U C G, long single helix
tRNA = ribose and phosphate backbone, A U C G, small single strand folded into clover shape, amino acid carried by extended chain, contains the anticodon to mRNA codon

21
Q

how is mRNA adapted for protein synthesis

A

acts as a template during protein synthesis:
mRNA codons code for amino acids to make polypeptides
easily broken down so only exists when required
single strand able to leave through nuclear pores

22
Q

how is tRNA adapted for its job

A

anticodon has complementary base pairing to codon on mRNA
carries an amino acid to form the polypeptide chain

23
Q

polypeptide synthesis: transcription

A
  • DNA helicase breaks hydrogen bonds between DNA bases so it uncoils and exposes the organic bases
  • free RNA nucleotides line up to ONE strand that acts as a template and pair with complementary bases
  • RNA polymerase joins the molecules together by phosphodiester bonds through condensation reactions to form pre-mRNA which then detaches from the dna
  • when a stop codon (last 3 bases on mRNA) is reached this ceases
24
Q

protein synthesis: splicing

A

pre-mRNA is spliced to remove the (non-coding) introns leaving only exons
mRNA contains no introns

when exons rejoin they do so in a variety of different combinations
- so a particular section of DNA can end up coding for a no of proteins depending on arrangement of exons after splicing

25
Q

protein synthesis: translation

A

once outside the nucleus:
- a ribosome attaches to the starting codon (AUG) at one end of the mRNA molecule
- the tRNA with the complementary anticodon sequence moves to the ribosome and pairs up with the codon on the mRNA. the tRNA carries a specific amino acid
- the ribosome moves along the mRNA bringing together two tRNA molecules at any one time, each pairing up with the corresponding two codons on the mRNA
- the two amino acids on the tRNA are joined by peptide bonds using an enzyme and ATP which is hydrolysed to provide the required
- the ribosome moves onto the 3rd codon, linking the amino acids on. the second and third tRNA molecules
- so the first tRNA molecule is released from its amino acid and is free to collect another one

26
Q

gene mutations def

A

any change to 1 or more nucleotide bases
or rearrangement of the bases in DNA

27
Q

how can mutations occur

A

natural - spontaneously during DNA replication (1-2 per 100,000 genes)

mutagens - high energy radiation disrupts DNA molecule, chemicals that alter DNA structure or interfere with transcription

28
Q

3 substitution mutations

A

non-sense mutation — a stop codon is produced, protein isn’t able to be made

mis-sense mutation — a different αα is produced

silent mutation — the same amino acid produced
(due to degenerate nature of the genetic code)

29
Q

deletion mutation

A

loss of a single nucleotide - due to the fact DNA is read in triplets, one deleted nucleotide causes all sequential triplets to be read differently as each has been shifted to the left by one base
(frame shift)

30
Q

binary fission in bacteria

A

circular DNA molecule replicates, both copies attach to cell membrane
plasmids also replicate
cell membrane grows between two DNA molecules and pinches inwards, diving cytoplasm into two
new cell wall forms between two molecules of dna diving original cell into two identical daughter cells, each with a single copy of the circular DNA and a variable number of copies of the plasmids