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BIOLOGY
Genetics
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Evie Robertshaw
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Definitions Genetics
BIOLOGY > Genetics
48 cards
Cards (287)
What 2 strands does DNA consist of?
Polynucleotide
strands
What
direction does the second polynucleotide chain run in?
Opposite
What
does RNA do?
Transfers genetic information from DNA to
ribosomes
What is messenger RNA?
A single stranded
copy
of one genes
DNA.
What does mRNA do?
Takes a
copy
of the gene out of the nucleus to the
ribosome
where it is used for protein synthesis.
What is transfer RNA?
Single
stranded molecule thats folds using
complementary
base pairing.
What does tRNA do?
Carries an
amino acid
to the
ribosome
to be made into a protein.
How many tRNA molecules are needed for 20 different amino acids?
20
What is rRNA?
Single
stranded molecule which folds using
complementary
base pairing
What structure does rRNA form part of?
Ribosome
What is a
gene
?
Section of
DNA
on a
chromosome
that controls a feature by coding for formation of a specific protein.
Allele
Alternative forms of a particular gene with different
base
sequences, coding for different versions of the same
protein
Structure
of chromosomes
DNA
molecule
DNA combined with
histone
DNA-histone
complex called
nucleosome
Nucleosomes
form
loops
Loops pack together to form
chromosomes
Formation
of chromosomes
1. DNA wrapped around
histone proteins
to form
nucleosomes
2.
Nucleosomes
form
chromatin loops
3.
Chromatin loops
wrapped around each other to form
full chromosome
Chromosomes are located within the
nucleus
and only visible as distinct structures when a cell is
dividing
Chromosome
structure during cell division
Appear as
2
threads (chromatids) joined by a single point (
centromere
)
Each thread is called a chromatid because the
DNA
has already replicated to give 2
identical
DNA molecules
Chromosome
Has
2
short arms (parms)
Has
longer
arms (franger arms)
Has a
centromere
holding it all together at the
lenne
Telomeres
Sections of
DNA
at the
ends
of each chromosome
Homologous
chromosomes
The number of chromosomes is always the same for individuals of the same
species
Humans always have
46
chromosomes arranged into
23
pairs
Genes
on a chromosome
Paternal -
13
different forms of the same gene
Maternal -
9
different forms of the same gene
Genes
are always located at the same portion (
locus
) on the same chromosome
Alleles
Slight differences in
DNA structure
that cause variation in
genes
A
karyotype
is the full chromosome complement, and illustrates the number,
size
and shape of the chromosomes
The
human male karyotype has 22 autosomes and
sex
chromosomes plus X,Y
The human female karyotype has 22 autosomes and
sex
chromosomes plus
XX
In human ordinary body cells, humans have
46
chromosomes - the
diploid
number
In gametes (sex cells) the number of chromosomes is
23
, the
haploid
number
Features
of the genetic code
It is a
triplet
code
3 bases =
1
amino acid
There are
20
different amino acids
4 DNA bases (adenine,
guanine
,
cytosine
, thymine) are used to achieve this
If there are
2
bases, it codes for only
16
amino acids
If there are 3 bases, it codes for
1
amino acid
Advantage
of triplet code
Allows for
mistakes
to be made in
DNA
sequence
Genetic
code
It is a
degenerate
code
Most amino acids are coded to by more than one
triplet
Only 2 amino acids have just one
triplet
code (
methionine
and tryptophan)
The start codon is always
methionine
, but the first
methionine
molecule doesn't form part of the final polypeptide chain and is later removed
There are 3 stop codons (do not code for any
amino acid
), and therefore mark the end of the
polypeptide
chain
Advantage
of degenerate code
If certain bases are changed, the
same
amino acid is produced
Genetic
code
It is a
non-overlapping
code
Each base appears only
once
in one
triplet
Can only read the base
once
Advantage
of non-overlapping code
If a mistake is made, it only affects
one
amino acid
The genetic code is
universal
, it is the same in
all
living things
Advantage
of universal code
Allows
insulin
producing bacteria to take the human
insulin
gene and produce human insulin
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