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prokaryotic DNA
shorter, circular, not associated with proteins, no introns
eukaryotic DNA
longer, linear, associated with proteins called histones, contains introns
eukaryotic DNA - MITOCHONDRIA + CHLOROPLASTS
-is like prokaryotic DNA
-is short, circular, no histones
SIMILARITIES between eukaryotic DNA + prokaryotic DNA
-nucleotide structure is identical
-nucleotides joined by phosphodiester bond
-DNA in mitochondria + chloroplasts is the same as prokaryotic
histones
-DNA in a chromosome is held by proteins called histones as it is very long
-the double helix is tightly wounded around histones which fix DNA in position
-DNA-helix complex is coiled and looped to form a single chromosome
gene
a sequence of DNA bases that codes for a polypeptide or functional RNA
-the base sequences are in triplets which determines the sequence of amino acids in primary structure
locus
the fixed position occupied by a gene on a DNA molecule
triplet
sequence of 3 DNA bases codes for 1 specific amino acid
genetic code
order of bases on DNA
-universal = the same triplet always codes for the same amino acid
-non-overlapping = each base is only part of one triplet
-degenerative = more than one triplet codes for each amino acid
reading genetic code
-triplets are read in one direction
-start codon = start of a sequence always has the same triplet
-stop codon = three triplets that mark the end of a sequence
types of DNA
-introns = DNA base sequence that does not code for a polypeptide - found between genes
-exons = DNA base sequence that codes for a polypeptide
alleles
alternative forms of the same gene
-found at the same locus and chromosome
-any change in a base sequence of a gene results in a new allele
homologous pairs
-two chromosomes that carry the same genes at the same loci
-but may carry different alleles
-have pairs of matching chromosomes
‘Explain how a change in a sequence of DNA bases could results in a non-functional enzyme’
-change in base sequence
-change in sequence of amino acids
-change in hydrogen bonds resulting in change of tertiary structure
-change in polypeptide so substrate cannot bind