deoxyribonucleic acid, a self-replicating material present in nearly all living organisms as the main constituent of chromosomes and is the carrier of genetic information.
a segment of DNA found on the chromosome that codes for a particular sequence of amino acids, which are put together to make a specific protein and thus determines a trait
why is understanding the human genome important for science and medicine?
- allows scientists to identify genes in the genome that are linked to different types of disease
- knowing which genes are link to inherited diseases could help us understand them better and could help us develop effective treatments for them
- the human genome is mostly identical in all individuals, but tiny differences have been developed as people migrated from the common ancestor and studying these differences can help scientists work out when new populations split off
there are parts of DNA that don't code for proteins - some of these non-coding parts switch genes on and off, so they control whether or not a gene is expressed (used to make a protein)
use the code in the DNA found in the nucleus, however it cannot move out of it due to its large size, so mRNA is used to get the code from the DNA to the ribosome
messenger RNA; type of RNA that copies and carries instructions from DNA in the nucleus to the ribosome - the correct amino acids are brought to the ribosomes in the correct order by carrier molecules
most have very little to no effect on the protein, some will change it to such a small extent that its function or appearance is unaffected and some mutations can seriously affect a protein, where it could change its shape and affect its ability to perform its function
where a new base in inserted into the DNA base sequence where it shouldn't be and this changes the way the DNA base sequence is read, which can change the amino acids they code for. insertions can change more than one amino acids acid as they have a knock-on effect on the bases further on in the sequence
when a random base is deleted from the DNA base sequence, changing the way the base sequence is read and has knock-on effects further down the sequence