Mod 6: RNA biology Flashcards
what is different about the chemical structure of RNA compared to DNA
contains 2’ - OH
whereas DNA lacks this group (hence deoxy)
also, no thymine, only uracil
see onenote for structure
what does this difference mean for the RNA’s stability?
makes it less stable than DNA
what is the difference between uracil and thymine
uracil doesn’t have the methyl group whereas thymine does
what are the 5 main roles of RNA
- transfer of info from DNA to proteins (via mRNA that codes for proteins)
- synthesis of proteins (via rRNA and tRNA)
- processing mRNA (small nuclear RNA i.e. snRNA, which is involved in splicing introns from pre mRNA)
- processing and modifying rRNA (via small nucleolar RNA i.e. snoRNA)
- catylitic RNA (e.g. self splicing introns, rybozymes)
how much RNA does a single cell contain in pg
10 picograms (10^-11 g)
what % RNA is ribosomal RNA
80-85%
what % RNA is low molecular weight (e.g. tRNA, snRNA etc)
10-15%
what % RNA is mRNA
1-5%
what part of the RNA is hydrophobic and which is hydrophilic
the ribose sugar and phsophate backbone is hydrophilic
the organic bases are hydrophobic
what does a strand of RNA do to increase its stability
uses self complementarity to form base pairs with itself to forms secondary structure
this makes base pads, kinda loops over on itself
gives it a tertiary structure
see onenote
how is the secondary structure formed
via palindromic sequences (ie self complementary bases)
which are seperated by a random sequence that isnt related
the slef complementary bases can loop over to pair to each other and form stem loop structure
see onenote
what is the name of the type of sequence that forms this secondary structure
hyphenated dyad symmetry
(hyphen cuz of the useless sequence in the middle of the two complementary sequences)
what are the 3 ways the usage/amount of RNA can be regulated
1) controlling the synthesis - its transcription, so whether or not it’s made, can be turned on and off rapidly
- e. g. lac operon
2) regulating its degradation - after its made, due to its lack of stability, if it’s not made stable it’ll just degrade away
- e.g. trnasferrin receptor mRNA
3) its translation effieciency - proteins can control the usage of certain RNAs
- e.g. ferritin mRNA
what region regulates the degradation of RNA and its translation efficiency?
UTR
transferrin receptors as an example of degradation regulation - see onenote for diagram and explanation
:)