genetic information Flashcards

1
Q

define gene

A

a sequence of DNA nucleotide bases that codes for a polypeptide or a functional RNA

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2
Q

structure of DNA

A

double stranded molecule
each strand is a polynucleotide made up of individual nucleotides

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3
Q

what is a DNA nucleotide composed of?

A

phosphate group
deoxyribose sugar
nitrogenous base

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4
Q

describe the DNA in prokaryotes

A

circular DNA
some have smaller loops of plasmid
DNA is naked
not associated with histone proteins

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5
Q

describe the DNA in eukaryotic chloroplasts and mitochondria

A

short circular molecule
not associated with histone proteins

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6
Q

describe the DNA in the nuclei of eukaryotic cells

A

very long linear molecule
associated with histone proteins
DNA molecule and histone proteins forms a chromosome

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7
Q

describe a homologous chromosome

A

-same genes of same loci
-centromeres at same place so same shape and size
-one maternal, one paternal

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8
Q

how is a chromosome formed?

A

-DNA molecule is wrapped around histone proteins to fix in place
-DNA histone complex is coiled into solenoids

this means a very long molecule of DNA can be condensed into a single chromosome (a lot of info)

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9
Q

what do humans have a diploid number of?

A

2n=46

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10
Q

what do genes code for?

A

either:
-the amino acid sequence of a polypeptide
-a functional RNA (including rRNA and tRNA)

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11
Q

where do genes occupy?

A

locus (fixed position)

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12
Q

what is an exon?

A

parts of a gene which codes for amino acid sequences

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13
Q

what are introns?

A

non-coding sequences

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14
Q

define genome

A

complete set of all the genes in a cell

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15
Q

define proteome

A

the full range of all the proteins that a cell is able to produce using its genome

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16
Q

define allele

A

two or more versions of a genetic sequence coding for a different polypeptide

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17
Q

define gene pool

A

all the different alleles of all the genes found within a population

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18
Q

which amino acid does the start triplet always code for

A

methionine

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19
Q

define triplet

A

every three bases in the sequence of a gene

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20
Q

what does a triplet code for?

A

a specific amino acid

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21
Q

how many different nucleotides are there in DNA?

A

4

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22
Q

how many possible combinations of triplets are there to code for 20 amino acids?

23
Q

define degenerate

A

in the genetic code, most amino acids are coded for by more than one triplet

24
Q

how many triplets dont code for amino acids in DNA?
what are they called?

A

3
stop triplets

25
define universal
the same triplet always codes for the same amino acid
26
define non-overlapping
each base is only read once, each base is part of only one triplet
27
RNA structure
single stranded polynucleotide nucleotides composed of phosphate,ribose sugar and nitrogenous base (Uracil instead of Thymine)
28
how long is messenger RNA?
few thousand nucleotides long
29
what is every 3 bases called in mRNA?
codon
30
what is the shape of mRNA?
linear molecule as bases don't bond to each other
31
how long is transfer RNA?
about 75 nucleotides long
32
describe the structure of tRNA
-strands fold back on themselves -hydrogen bonds form between complementary base pairs -shape is called clover leaf -one end is an amino acid binding site -3 of the bases are exposed called an anticodon
33
how many different types of tRNA are there?
61
34
why are there not 64 triplets?
because there are 3 stop codons which dont code for any specific amino acid
35
how is a protein made in eukaryotes?
-specific gene is transcribed (introns and extrons) -this makes pre-mRNA -this is spliced to form mRNA -this is a copy of the exons of the gene only -mRNA is translated to make polypeptides
36
describe transcription in the nucleus
-gene unwinds as hydrogen bonds between complementary bases broken by RNA polymerase -one strand acts as a template -complimentary free RNA nucleotides bind to exposed bases -in a condensation reaction, sugar phosphate backbone is joined using RNA polymerase -both inton and exon are transcribed to make pre-mRNA
37
what disengages the RNA polymerase?
the stop triplet marking the end of a gene
38
describe splicing in eukaryotic cells
pre-mRNA is spliced the non-coding sections (transcribed from the introns) are cut out and coding sections are edited together to produce mRNA
39
what types of DNA dont need splicing? why?
prokaryotic DNA chloroplast and mitochondria DNA because they dont have introns
40
where does translation happen? and what does it make?
cytoplasm makes polypeptides
41
describe translation
-mRNA moves out of nucleus and attaches to ribosome. -tRNA carrying amino-acids bind by their anticodons to the mRNA - by complementary base pairing. -Another molecule of tRNA with another amino-acid attaches to the mRNA on the next codon along. - The two amino-acids on the tRNA form a peptide bond. -The first tRNA now moves away and a new tRNA attaches. - This process repeats, adding more amino-acids to the polypeptide-chain. -Process ends when a 'stop signal' is reached and completed polypeptide detaches.
42
what does a gene mutation involve?
a change in the base sequence of a chromosome
43
what are neutral mutations?
when the change in amino acid sequence does not affect the function of the protein
44
why might some substitutions not result in any change?
genetic code is degenerate the new triplet may code for the same amino acid
45
what are silent mutations?
in substitution mutation when the mutation causes no change
46
what happens to the length of the polypeptide chain when the new triplet is a stop triplet?
shorter
47
what does addition result in?
a frame shift
48
what's the consequence of a frame shift?
new sequence of amino acids changes position of hydrogen and disulphide bonds
49
what 2 mutations result in a frame shift?
addition deletion
50
how can the rate of mutations be increase?
mutagenic agents
51
x4 examples of mutagenic agents?
-high energy radiation -ionising radiation -chemicals eg tar in cigarette smoke -viruses
52
what are carcinogens?
substances which cause mutations in oncogenes which cause the cell to become cancerous
53
whats non-disjunction?
when homologous chromosomes do not separate in meiosis
54
whats down syndrome caused from?
non-disjunction of chromosome 21