Story of Us : part 2 Flashcards
what does DNA contain?
- the information needed to make a protein
what codes for a specific amino acid?
- three bases (a codon)
what is the sequence of bases?
- a set of instructions for which order to join amino acids in to make a protein
what is mRNA?
- a copy of DNA
what does mRNA do?
- moves from the nucleus to the ribosomes where proteins are synthesised in the cytoplasm
-the protein produced depends on the sequence of bases in the mRNA, and if this sequence changes, a different protein will be made
what is tRNA?
- carrier molecules
what does tRNA do?
- brings specific amino acids to add to the growing protein in the correct order
how many amino acids are there?
- only about 20 differently naturally-occurring amino acids
how many amino acids are there in each protein molecule?
- has hundreds or even thousands of amino acids joined together in a unique sequence
what has to happen to the unique sequence of amino acids?
- folded into the correct unique shape
- this is v important as it allows the protein to do its job
what jobs do proteins have?
- some proteins are enzymes, others are hormones and others form structures within the body, such as collagen
- each of these proteins needs a different shape
how do cells express their genes?
- by converting the genetic message into protein
what two stages does the process of protein synthesis occur in?
- transcription
- translation
what is transcription?
- when a gene is to be expressed, the sequence of bases in RNA is copied or transcribed into mRNA (messenger RNA)
- this process takes place in the nucleus and occurs in a series of stages
describe transcription.
- the two stands of DNA helix are unzipped by breaking the weak hydrogen bonds between base pars. the unwinding of the helix is caused by an enzyme (helicase)
- the enzyme RNA polymerase attaches to the DNA just before the gene
- RNA polymerase moves along the DNA strand. free RNA nucleotides are attracted to (and form hydrogen bonds with) the exposed DNA strand nucleotides by complementary base pairing
- RNA polymerase then catalyses the formation of covalent bonds between the RNA nucleotides to form a strand of mRNA
- the newly formed of mRNA is now ready to leave the nucleus and travel to the ribosome
what are the bases of RNA nucleotides?
- contain the same bases as DNA, except that T is replaced by U. U base pairs with A
- because the opposite base bonds with the exposed DNA bases, the strand of mRNA is an opposite copy of the DNA strand (except that U replaces T).
- we call this a complementary copy
describe translation.
- the mRNA strand travels through the cytoplasm and attaches to the ribosome. the strand passes through the ribosome.
- for every three mRNA bases the ribosome lines up one complementary molecule of tRNA. we call every three bases on mRNA a codon. the complementary three bases on the tRNA are an anticodon. e.g. if CGG is the mRNA codon, the tRNA anticodon is GCC - the triplet code
- tRNA molecules transport specific amino acids to the ribosome. the ribosome allows two tRNA molecules to sit next to each other; the ribosome catalyses the formation of a covalent bond (peptide bond) between the two amino acids.
- used tRNA molecules exit the ribosome and collect another specific amino acid
- a chain of several hundred amino acids forms in the correct order according to the original DNA is then made. this is called a polypeptide
what happens after translation?
- the polypeptide is finally folded into the correct shape and becomes a protein
what is a result of sexual reproduction?
- variation in genes
- new forms of genes can result from mutations
what is a mutation?
- a change in the sequence of bases in DNA
what would cause a change in the sequence of bases in DNA?
- this can be due to the replacement of a single base pair with a different pair, or an addition or deletion of one or more base pairs.
- this gives a change in the DNA sequence which in turn changes the sequence of amino acids in the protein
- this will normally alter the shape and function of the protein
what is chromosomal mutation?
- when a cell gains an extra chromosome (such as Down’s Syndrome) or one part of a chromosome is stuck onto another chromosome
are mutations common in eukaryotes?
- mutations are comparatively rare events in eukaryotes as our cells can detect and correct many mistakes in the DNA sequence
are chromosomal mutations harmful?
- they are almost always harmful, as they result in over or underproduction of proteins
are changes in the DNA sequence harmful?
- changes in the DNA sequence are often neutral , meaning they have no effect, but can less often be either positive, ie increasing variation and my be beneficial if the environment changes, or negative ie the proteins failing to work properly
what happens if the mutation occurs during meiosis?
- if the mutation occurs during meiosis in gamete formation it will affect all of the cells in the individual which develops from the gamete
- this means that the mutation is inherited