C4 - DNA AND RNA Flashcards
is DNA stored the same or differently in prokaryotic and eukaryotic cells
differently
how is DNA stored
- STRUCTURE of DNA is the same in all organisms
- they way DNA is STORED is different in eukaryotes and prokaryotes
how is DNA stored in eukaryotic cells
- cells contain linear DNA molecules that are CHROMOSOMES
- each chromosome is made of 1 long molecule of DNA and its associated proteins
- chromosomes are found in the NUCLEUS
- DNA molecule is really long, so it needs to be wound up so it can fit into the nucleus
- DNA is wound around HISTONES
- histone proteins also help to support the DNA
- DNA is coiled up very tightly to make up a compact chromosome
what is DNA like in the mitochondria and chloroplasts in eukaryotic cells
- have their own DNA
- similar to prokaryotic DNA because its CIRCULAR AND SHORTER than the DNA molecules in the nucleus
- NOT assosciated with histone proteins
what is DNA like in prokaryotic cells
- also carry DNA as chromosomes
- DNA molecules are shorter and circular
- DNA is NOT wound around histones
- instead it condenses to fit into the cell by SUPERCOILING
does a small or large amount of the DNA in a cell carry genetic info
a small amount
what is the most important part of DNA
genes
what are genes
a sequence of DNA bases that codes for a polypeptide or functional RNA
what does the sequence of amino acids code for in a polypeptide
the primary structure of a protein
what is the reason for polypeptides differing from eachother
- a different number and order of amino acids
what does the order of bases in a gene determine
the order of amino acids in a polypeptide
what is a triplet/codon
- codes amino acids
- is a sequence of 3 bases in a gene
describe how polypeptides are made in a very basic way
- DNA is first copied into mRNA (messenger RNA)
- first stage of protein synthesis
if genes dont code for a polypeptide, what do they code for
functional RNA
what is functional RNA
- RNA molecules other than mRNA
- they perform special tasks during protein synthesis
- ex, tRNA and rRNA (ribosomal RNA)
what is the term for a full set of genes in a cell
genome
what is the term for a full set of proteins that a cell is able to produce
proteome
what is non coding DNA
- genes that do code for polypeptides contain sections which dont code for amino acids : this is non coding DNA
what is the term for non coding DNA
- introns
- (think of intervals, like adverts, in a movie - not part of the movie)
describe introns
- non coding DNA
- can be several introns in a. gene
- purpose is NOT known
what happens to introns in eukaryotes
- removed during protein synthesis
- as they are removed, they dont affect the amino acid order
what happens to introns in prokaryotes
- prokaryotic DNA does NOT contain introns
what is the term for the parts of a gene which do code for amino acids
exons
what are non coding multiple repeats
- in eukaryotic DNA
- regions of multiple repeats outside of genes
- DNA sequences that repeat over and over
- these areas dont code for amino acids
- ex, CCTTCCTTCCTTCCTT
what are alleles
- a gene can exist in more than one form : alleles
- order of bases in each allele is slightly differently, therefore they code for slightly different versions of the same polypeptide
what are homologous chromosomes
- in a eukaryotic cell nucleus, DNA is stored as chromosomes
- humans have 23 pairs of chromosomes = 46 in total
- pairs of matching chromosomes = homologous pairs
- in a homologous pair, both chromosomes are the same size and have the same genes, however they can have different alleles
- alleles coding for the same characteristics will be found at the same fixed position (LOCUS) on each chromosomes in a homologous pair
how many types of RNA play a key role in protein synthesis
2
what are the 2 types of RNA that play a key role in protein synthesis
- mRNA
- tRNA
what is protein synthesis
- the production of proteins/polypeptides from the info contained in the cells DNA
- also called polypeptide synthesis
- involves both transcription and translation
what is transcription
where the DNA code is copied into mRNA
what is translation
where the mRNA joins with a ribosome and the code it carries is used to synthesise a protein
what is RNA
- a single polynucleotide strand
- bases : A, U, C and G
- A and U pair during protein synthesis
- C and G pair
- 2 types of RNA : mRNA and tRNA
what is mRNA
- messenger RNA
- made during transcription
- carries the genetic code from the DNA -> ribosomes : used to make PROTEIN during TRANSLATION
- mRNA is a single polynucleotide strand
- 3 adjacent bases in mRNA are called CODONS (sometimes called triplets or base triplets)
what is tRNA
- transfer RNA
- involved in translation
- carries the amino acids used to make proteins -> ribosomes
- tRNA is a single polynucleotide strand folded into a CLOVER shape
- hydrogen bonds between specific base pair holds the molecule in this shape
- every tRNA molecule has a specific sequence of 3 BASES at one end : ANTICODON
- opposite end has an AMINO ACID BINDING SITE
how are proteins synthesised
using the instructions in DNA
what 2 steps takes place in protein synthesis
- transcription
- translation
simply describe what happens in transcription
- an mRNA copy is made from DNA
where does transcription take place in eukaryotic cells
nucleus
where does transcription take place in prokaryotic cells
because they have no nucleus, it takes place in the CYTOPLASM
describe how transcription takes place
- RNA polymerase attaches to the DNA double helix at the start of the gene
- in eukaryotes, the hydrogen bonds between the 2 DNA strands in the gene are broken by the DNA HELICASE attached to the RNA polymerase
- 2 strands are separated and the DNA molecule uncoils -> this exposes some of the bases
- one of these strands is used as a template strand
- the RNA polymerase lines up free RNA nucleotides alongside the exposed bases on the template strand
- specific complementary base pairing causes the mRNA to be a complementary copy of the DNA template strand (but thymine is replaced with uracil)
- once RNA nucleotides have paired up with their specific bases on the DNA strand, they are joined up by RNA polymerase -> forms mRNA strand
- RNA polymerase moves along the DNA strand, assembling the mRNA strand
- the hydrogen bonds between the uncoiled strands of DNA reform once the RNA polymerase has passed by it
- strand coils back into a double helix
- when RNA polymerase reaches a stop signal, a particular DNA sequence, it STOPS making mRNA and then detaches from DNA
- in eukaryotes, mRNA moves out of the nucleus through the nuclear pore and attaches to a ribosome in the cytoplasm, then translation takes place
how are the DNA strands separated in prokaryotes
by RNA polymerase
are free RNA nucleotides attached to anything
no
they are freely floating in the nucleus
does transcription produce the same or different products in eukaryotes and prokaryotes
different products
what is mRNA like in eukaryotes prior to splicing
- both introns and exons are copied into mRNA during transcription
- mRNA strands contain introns and exons = pre mRNA
what is splicing and what happens in it
- splicing is where introns are REMOVED and the exons are joined together
- this forms mRNA strands
- takes place in the nucleus
- the mRNA leaves the nucleus after this, for translation
does prokaryotic mRNA go through splicing
- mRNA is produced DIRECTLY from DNA, therefore splicing does not take place
- no need for splicing as there are no introns in prokaryotic DNA
what is translation in simple terms
- second stage of protein synthesis
- takes place in RIBOSOMES in both eukaryotes and prokaryotes
- during translation, amino acids are joined together to make a polypeptide chain
describe the process of translation
- the mRNA attaches itself to a ribosome and tRNA molecules carry amino acids to it
- ATP provides the energy needed for the bond to form between the amino acid and tRNA molecule
- a tRNA molecule, which carries an amino acid, with an anticodon thats complementary to the first codon on the mRNA - it attaches itself to the mRNA by complementary base pairing
- a second tRNA molecule attaches itself to the next codon on the mRNA in the same way
- the 2 amino acids attached to the tRNA molecules are joined by a PEPTIDE BOND
- first tRNA molecule moves away, leaving its amino acid behind
- a third tRNA molecule binds to the next codon on the mRNA
- its amino acid binds to the first 2 and the second tRNA molecule moves away
- this process continues and produces a chain of linked amino acids until there is a stop signal on the mRNA molecule
- PP chain moves away from the ribosome and translation is complete
what is another name of protein synthesis
polypeptide synthesis
give an example of the codon on the mRNA which is complementary to the anticodon on tRNA
anticodon on tRNA = UAC
codon on mRNA = AUG
what is the genetic codes purpose
encodes info in genes which determine what we look like, how we develop
what is the genetic code
- sequence of base triplets (codons) in mRNA which code for specific amino acids
- each base triplet is read in sequence, separate from the triplet before and after it
what does non overlapping mean in context of the genetic code
base triplets dont share their bases
what does degenerate mean in context of the genetic code
- there are more possible combinations of triplets than there are amino acids
- some amino acids are coded for by more than one base triplet
- not all triplets code for amino acids
there are only 20 amino acids, but how many possible triplets from these
64
what are stop signals
- triplets which are used to tell the cell when to stop production of a protein
- found at the end of mRNA
give an example of a stop signal and its purpose
UAG
what is a start signal
- at the start of mRNA
- tell the cell when to start protein production
- code for a specific amino acid called methionine
what does universal mean in the context of the genetic code
- the same specific base triplets code for the same amino acids in all living thing
- ex, UAU codes for TYROSINE in all organisms
what is a gene mutation
- change in the base sequence of DNA
- can arise spontaneously in DNA replication (in interphase specifically)
- ex, base deletion or substitution
what is a mutagenic agent
a factor that increases the rate of genetic mutation
give an ex of a mutagenic agent
- UV light
- alpha particles
how can a mutation lead to the production of a non - functional protein or enzyme
- changes sequence of base triplets in DNA/in a gene = changes codons on mRNA
- therefore changes sequence of amino acids in the PP
- therefore changes position of hydrogen/ionic/dispute bonds between amino acids
- therefore changes the TERTIARY structure of the protein
- in enzymes, this causes the active site changes shape so the substrate cant bind and therefore an E-S complex cant form
what are the possible effects of a substitution mutation
- base/nucleotide is replaced by a different base/nucleotide
- changes one triplet = changes one mRNA codon
- one amino acids in PP changes -> can cause the tertiary structure to change if the position of H/I/D bonds change
OR
- amino acid does NOT change due to the degenerate nature of the genetic code (triplet could code for the same amino acid) OR if the mutation is in an intron (gets spliced and introns are non-coding DNA anyways)
explain the possible effects of a deletion mutation
- one nucleotide/base is removed from the DNA sequence
- changes the sequence of DNA triplets from the point of mutation -> FRAMESHIFT
- changes the sequence of mRNA codons after the point of mutation
- changes the sequence of the amino acids in the PRIMARY structure of the PP
- changes the position of H/I/D bonds in TERTIARY structure
- changes the TERTIARY structure/shape of protein
what are homologous chromosomes
- same length
- same genes at same loci
- may have different alleles
what is a diploid cell
- have 2 complete sets of chromosomes
- represented as 2n
- DIPLOID = DOUBLE = 2
what is a haploid cell
- has a SINGLE set of unpaired chromosomes
- represented as n
what happens in interphase for meiosis
- DNA replicates
- 2 copies of each chromosome (sister chromatids) joined by a centromere
what happens in meiosis 1
- first nuclear division
- separates homologous chromosomes
steps
- chromosomes arrange into homologous pairs
- crossing over between homologous chromosomes
- independent segregation of homologous chromosomes
what happens in meiosis 2
- second nuclear division
- separation of chromatids due to centromere being split
what is produced from meiosis
- 4 genetically VARIED daughter cells
- daughter cells are normally HAPLOID (if the parent cell is diploid)
why is the number of chromosomes halved during meiosis
as homologous are separated during meiosis 1
how does crossing over create genetic variation
- homologous pairs of chromosomes associate/form a bivalent
- chiasmata form (point of contact between non sister chromatids)
- alleles/lengths of non sister chromatids are exchanged between chromosomes
- results in the creation of new combinations of maternal and paternal alleles on chromosomes
how does independent segregation creates genetic variation
- homologous pairs randomly align at equator -> random which chromosome from each pair goes into each daughter cell
- creates different combinations of maternal and paternal chromosomes/alleles in daughter cells