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Miss Estruch
Topic 4
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Gene
: a section of DNA that contains a code for making a
polypeptide
and
functional RNA
Locus
: the
location
of a particular gene on a chromosome
Allele
: a different
version
of the same gene
Chromosome
:
threadlike structure
composed of
tightly coiled DNA
wrapped around histones (if it is a eukaryotic cell)
Homologous chromosome
: a pair of chromosomes that
have the same
genes therefore, they are the same
size
Eukaryotic
DNA:
DNA is stored as
chromosomes
inside
the
nucleus
linear chromosomes
DNA is tightly coiled and wrapped around proteins called
histones
Prokaryotic
DNA:
DNA molecules are
shorter
and
circular
DNA is not wound around histones. Instead, it
supercoils
to fit in the cell
Codon
:
3
bases on
mRNA
that code for an
amino acid
Start
codon
:
3
bases at the start of an mRNA sequence which help to
initiate
translation
Genetic
code: an amino acid is coded for by
3
DNA bases
which are described as the "
triplet code
"
What is the advantage of the genetic code being
universal
?:
genetic
engineering
is possible
a human gene can be inserted into another organism
e.g human gene for insulin inserted into bacteria to make insulin
What is the advantage of the genetic code being
non-overlapping
?: if a point mutation occurs, it will
only
affect
one codon
and therefore one amino acid
Triplet
code: an amino acid is coded for by
3
bases
Mutation
:
a change in the
DNA
can be a
gene
or
chromosome
mutation
What is meant by 'the genetic code is
universal
?'
the
same triplet
of
bases
codes for the
same
amino acid
in all organisms
What is meant by 'the genetic code is
non-overlapping
?:
each base in a gene is only part of
one triplet
of
bases
that codes for one amino acid
therefore each codon is read as a
discrete unit
What is
splicing
?:
post-transcription modification
removing
introns
Genome
: the complete
set of genes
in a cell
Proteome
: The full range of
proteins
that a
cell
is
able
to
produce
Anticodon
:
3
bases on the
tRNA
which are
complementary
to the
codon
on mRNA.
tRNA
structure:
single-stranded, folded to create a
cloverleaf
shape
held in place by
hydrogen bonds
has an
anticodon
and
amino acid
binding
site
mRNA
function:
a copy of a gene from DNA
created in the nucleus, and it then leaves the nucleus
to
carry the copy
of the
genetic
code
of one gene to a
ribosome
in the cytoplasm
tRNA
function:
a
specific
amino
attaches
at the
binding
site
transfers
this amino acid to the ribosome to create the
polypeptide
chain
Transcription
:
the
first
stage in
protein synthesis
one gene in DNA is copied into
mRNA
occurs in the
nucleus
Translation
:
the
second
stage in
protein synthesis
the
polypeptide
chain is
created
using both the mRNA base sequence and the tRNA
occurs on
ribosomes
in the cytoplasm
Which enzymes are involved in transcription?
DNA
helicase
RNA
polymerase
RNA polymerase
: joins
adjacent
RNA
nucleotides
together forming a
phosphodiester bond
pre-mRNA
: mRNA in
eukaryotes
that still contains the
introns
How is premRNA modified?
the
introns
are
removed
by a protein called a spliceosome
this leaves just the
exons
What is ATP used for in translation? forming the
peptide bond
between amino acids
Haploid
:
one copy
of each chromosome in a cell
Diploid
:
two copies
of each chromosome in a cell
Meiosis
:
cell division that creates genetically
different
gametes
there are two nuclear divisions in this process
results in
four
haploid
daughter cells
Independent segregation
:
homologous pairs
of
chromosomes
randomly line up opposite each other at the equator of the cell
when they separate it creates a
large
number
of
possible combinations
of
chromosomes
in the daughter cells produced
Crossing over
:
homologous
pairs
of chromosomes line up opposite each other at the equator in
meiosis 1
parts of the
chromatids
twist,
break
and
recombine
with another chromatid
results in new
combinations
of
alleles
in the
gametes
Gametes
: sex cells (sperm and egg)
What is a
frameshift
?:
the removal of one base
changes
all of the subsequent
codons
all the bases shift
back
one position
Chromosome
mutation:
change in the
number
of
chromosomes
occurs during
meiosis
Deletion
mutation:
a
gene
mutation
a base is removed from a sequence
causes a
frameshift
Substitution
mutation:
a
gene
mutation
a base is
swapped
for a different one
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