Genetic information, variation & relationships Flashcards
(44 cards)
gene
a DNA base sequence that codes for the amino acid sequence of a polypeptide or a functional RNA like tRNA
locus
the location of a particular gene on a chromosome
allele
a version of a gene
chromosome
a long, coiled molecule of DNA
homologous chromosomes
pairs of matching chromosomes
they are the same size and have the same genes, but may have different alleles
the genetic code as degenerate
each amino acid can be coded fro y more than one triplet of bases
why is it a benefit for the genetic code to be degenerate
if a point mutation occurs, even though the triplet of bases will be different, it may still code for the same amino acid
the genetic code as universal
the same triplet of bases codes for the same amino acid in all organisms
why is the genetic code being universal an advantage
it means genetic engineering is possible
making recombinant DNA e.g. inserting a human gene into bacteria
the genetic code as non-overlapping
each base in a gene is only part of one triplet of bases that codes for one amino acid
each codon is read as a discrete unit
why is the genetic code being non-overlapping an advantage
if a point mutation occurs, it will only affect one codon, therefore one amino acid
introns
sections of DNA that do not code for amino acids
they are found in eukaryotic DNA but not prokaryotic DNA
they are spliced from mRNA molecules
genome
the complete set of genes in a cell
proteome
full range of proteins a cell/organism is able to produce
transcription
DNA helicase breaks the hydrogen bonds between complementary base pairs, causing the DNA helix to unwind to expose the bases to act as a template
free RNA nucleotides in the nucleus align opposite to their complementary base pair
RNA polymerase bonds together the RNA nucleotides by forming phosphodiester bonds
translation
pre-mRNA is modified - spliced to remove introns
the mRNA eaves the nucleus and attaches to a ribosome in the cytoplasm
the ribosome attaches at the start codon
the tRNA molecule with the complementary anticodon to the start codon aligns opposite the mRNA
the ribosome moves along the mRNA molecule, allowing another complementary tRNA molecule to attach to the next codon
the two amino acids are joined by a peptide bond, requiring an enzyme and ATP
the ribosome has two binding points
this continues until the ribosome reaches the stop codon, where it detaches
the polypeptide chain enters the Golgi body for post-translational modifications
how can genetic variation be introduced
meiosis, mutation, and random fertilisation of gametes
crossing over
crossing over occurs in meiosis I
homologous pairs line up opposite each other at the equator and equal lengths of the non-sister chromatids twist around each other
this puts tension on the chromatids so they break at the chiasmata
the broken parts recombine with the other chromatid
this results in new combinations of alleles in the gametes
independent segregation
in meiosis I homologous pairs of chromosomes line up opposite each other at the equator of the cell
it is random which side of the equator the paternal and maternal chromosomes from each homologous pair lie
these pairs are separated, so one of each homologous pair ends up in the daughter cell
this creates a large number of possible combinations of chromosomes in the daughter cells produced
how is the total no. possible combinations of chromosomes calculated
2n
n = number of homologous pairs
silent mutation
the new codon still codes for the same amino acid as the genetic code is degenerate
chromosomal non-disjunction
the chromosomes or chromatids do not split equally during anaphase
polyploidy
changes in whole sets of chromosomes
aneuploidy
changes in the number of individual chromosomes