4 - DNA, RNA And Classification / Variation Flashcards
What are the 4 bases
Adenine
Thymine
Guanine
Cytosine
What are histones
Proteins that DNA get wound around
What charge is DNA
Slightly negative
What charge are histones
Slightly positive
What is the combination of DNA and histones called
Nucleosome
What is gene expression
Characteristic functional in a phenotype
DNA is wrapped + coiled around histone proteins to form a substance called what?
Chromatin
Do prokaryotes have histones
No
Why do prokaryotes not have histones
More simple
Usually smaller genomes as Si plaid functions
How does DNA exist in prokaryotes
DNA is circular, free in cytoplasm in 2 forms
- circular chromosomes
- small amounts in circular plasmids
Are mitrochondria and chloroplasts found in both prokaryotes and eukaryotes
No
Only eukaryotes as memebrane bound
Do mitochondria and chloroplasts have their own DNA
Yes
Eukaryotic cells contain …………. DNA that exist as ………….
Linear
Chromosomes
Where are chromosomes found in a eukaryotic cell
Nucleus
What has to happen to DNA so that it can fit into the nucleus and why
It’s very long so wound up
Are histones protines?
Yes
What do histone proteins do
Support the DNA
Do prokaryotes carry DNA in chromosomes
Yes
Describe the DNA molecules in prokaryotes
Shorter
Circular
Isn’t wound around histones
How does DNA in prokaryotes fit into cells
Supercoiling
What is a gene
A sequence of DNA bases that codes for either a polypeptide or functional RNA
The sequence of amino acids in a polypeptide forms the ………….. of a protein
Primary protein
What determines the order of amino acids in a particular polypeptide
The order of bases in a gene
What is each amino acid coded for by
three bases in a gene called a triplet
What is the first stage of protein synthesis
DNA is first copied to messenger RNA
Genes that don’t code for a polypeptide code fro what
functional RNA
What is functional RNA
RNA molecules other than mRNA, which preform special tasks during protein synthesis, and ribosomal RNA, which forms part of ribosomes
What is a called genome
The complete set of genes in the cell.
What is a cells proteome
The full range of proteins that the cell is able to produce
What are introns
In eukaryotic DNA, genes that do code for polypeptides contain sections that don’t code for amino acid , called introns
Can there be several introns within a gene
Yes
What are exons
Bits of a gene that do code for amino acids
Introns are ……… durning protien synthesis and why
Removed
So they don’t affect the amino acid order
Does prokaryotic DNA have introns
No
Eukaryotic DNA also contains regions of multiple repeats outside of genes, what does this mean
These are DNA sequences that repeat over and over
In eukaryotic DNA do multiple repeated outside of genes code for amino acids, so what are they called
No
Non coding repeats
What is an allele
A form of a gene
Why does each allele have slightly differnt versions of the same polypeptide
The order of bases is slightly differnt
How many pairs of chromosomes do humans have
23 pairs
What are pairs of matching chromosomes called
Homologous pairs
Describe homologous pairs
Both chromosomes are the same size and have the same genes, although the pay could have differnt alleles.
Alleles coding fro the same characteristics will be found at the same fixed position (locus) on each chromosome in anhomologous pair
Centre of a chromosome name
Centromere
What is an allele
Version of a gene
What is a gene
Section of DNA that codes for a particular characteristics
What is loci
Location of the gene in a chromosome
What is a chromosome
DNA in nucleus of eukaryotic cells is linear and arranged in chromosomes
What is chromatin
DNA wrapped and coiled around histone proteins
What does DNA stand for
Deoxyribose nucleic acid
What is a polypeptide
Chain of amino acid connected by peptide bonds
in prokaryotes, DNA isn’t wound around histones so how does it fit in the cell
Condenses by supercoiling
What is a codon
Sequence of 3 DNA / RNA nucleotides that correspond with a specific amino acid
What are exons
Code for an amino acid
What are introns
Don’t code of amino acids
(Removed during protein synthesis )
Does prokaryotes have both exons and introns
only exons
What. Happens first transcription or translation
Transcription
Where does transcription happen
In the nucleus
Where does translation happen
In the cytoplasm by the ribosome
What is splicing
Process of cutting out introns
Leaving on exons
What does a mRNA triplet code match to
A specific amino acid
What is a codon
mRNA strand being read in triplets
Where is an anticodon found
On tRNA
Explain transcription
The hydrogen bonds in the DNA, between complementary base pairs, is broken by an enzyme.
• two exposed strands, one used as a template.
- One of the DNA strands is used as a template to make the mRNA molecule, the template is called the antisense strand.
- Free nucleotides line up by complementary base pairing and adjacent nucleotides are joined by phosphodiester bonds thus forming a molecule of mRNA.
• The enzyme RNA polymerase catalyses the formation of phosphodiester bonds. - When a stop codon is reached this ceases. As the RNA polymerase moves away the DNA rejoins, with only 12 bases being exposed at a time to reduce the chance of damage to the DNA.
- In eukaryotic cells the pre-mRNA is then spliced to remove the introns leaving just a strand of exons.
- The mRNA then moves out of the nucleus through a pore and attaches to a ribosome in the cytoplasm which is the site of next stage of protein synthesis called translation.
What is broken in DNA during transcription to expose the 2 strands
Hydrogen bonds between complementary base pairs.
What is the template strand in transcription called
Antisense strand
How do adjacent nucleotides join up and for a mRNA molecule
And what is the catalyst
Phosphodiester bonds
Enzyme RNA polymerase catalysed
When does the RNA polymerase move away and the DNA rejoins in transcription
When a stop codon is reached
How many bases on DNA are exposed at one time in transcription
And why
12
To reduce chance of damage to DNA
What happens to pre-mRNA to produce mRNA
Splicing to remove introns
How does mRNA exit the nucleus
And where does it go
Through a nuclear pore
and attached to a ribosome in the cytoplasm
Why is DNA kept in the nucleus during protien synthesis
It’s more prone to damage ( mutations) outside the nucleus
Describe translation
- mRNA attaches to a ribosome
- transfer RNA collects amino acids from the cytoplasm and carries them to the ribosome.
• can only carry one type of amino acid, and a triplet of bases (anticodon) at the other. - tRNA attaches itself to mRNA by complementary base pairing
• two molecules attach to mRNA at a time. - The amino acids attached to two tRNA molecules join by a peptide bond and then tRNA molecules detach themselves from the amino acids, leaving them behind.
- This process is repeated thus leading to the formation of a polypeptide chain until a stop codon is reached on mRNA
• this ends the process of protein synthesis.
A ribosome can join up to 15 amino acids per second until the stop codon is reached. Furthermore up to 50 ribosomes can move along the same strand of mRNA behind one another so that several proteins can be assembled simultaneously.
What is the simplifed definition of translation
Amino acids join together to form a polypeptide chain
How many tRNA molecules can attach to mRNA at one time
2
What is the bond between 2 amino acids
Peptide bond
Is tRNA single or double stranded
Single
Describe the length of
DNA, mRNA and tRNA
DNA - long
mRNA- variable
tRNA- short
What shape is mRNA
Single helix / strand
What is the shape of tRNA
Clover
What type of sugar is in DNA
Deoxyribose
What type of sugar is in mRNA
Ribose
What type is sugar is in tRNA
Ribose
What bases are in DNA
Adenine (check )
Thymine
Cytosine
Guanine
What bases are in mRNA and tRNA
Adenine
Uracil
Cytosine
Guanine
Is DNAs quantity Large or small and is it constant
Large and constant
is mRNA quantity large or small and is it constant
Smaller
Varies
is tRNA quantity large or small and is it constant
Smaller
Varies
What is the stability in
DNA, mRNA and tRNA
DNA - stable
mRNA - unstable
tRNA - relatively stable.
How many possible triplets are there
And how many AA are there
64
20 AA
What are the features of the genetic code
non-overlapping: meaning that each triplet is only read once and triplets don’t share any bases.
• Genes are separated by non-coding repeats of bases.
• is degenerate: meaning that more than one triplet codes for the same amino acid,
What does genetic code being degenerate reduce
Mutations
homologous pairs consist of ……. Chromosomes that carry the same gene
But they arnt identical, why?
2
They can carry differnt alleles of the same gene
What sex chromosomes do females have
2 X chromosomes
What sex chromosomes do males have
X and Y chromosome
What does homologous pair of chromosomes contain
Contain the same set of genes
What 3 groups are in an amino acids
Carboxylic acid
Amino group
r group changes
What is required to form the bond between amino acids and tRNA molecule to from
And where else is thus required in translation
ATP
To join 2 amino acids together
What is the genetic code
The sequence of base triplets (codons) in mRNA which codes for specific amino acids
What does it mean that the genetic code is universal
The same specific base triplets code for the same amino acid in all living things
What are gametes
The sperm and eggs cells
They join togetehr during fertilisation to from a zygote
Which divides and develops into a new organism
How many chromosomes do normal body cells have (in humans)
What is the term to describe thus
46
Diploid
How many chromosomes are in the gametes in humans
And what is the term to describe this
23
Haploid
T or f
Fertilisation is random
T
What does random fertilisation produce
Zygotes with differnt combinations of chromosomes to both parents
What increases genetic diversity within species
The mixing of genetic material in sexual reproduction
Where does meiosis happen
In reproductive organs
What happens before meiosis starts
The DNA unraveled and replicates so there are two copies of each chromosomes called chromatids
The DNA then condensed to from double armed chromosmes, each made form 2 sister chromatids. The sister chromatids are joined in the middle by a centromere
How are 2 sister chromatids joined
By a centromere
Describe meiosis 1
The chronometer arrange themselves into homologous pairs
These homologous pairs are then separated halving the chromosome number
Describe meiosis 2
The pairs of sister chromatids that make up each chromosome are separated (the centromere is divided)
What is the product of meiosis
4 haploid cells that are genetically differnt from each other are produced
What can happen to chromatids in meiosis 1
homologous pairs of chromosomes come togetehr and pair up
The chromatids twist around each other and bits of the chromatids swap over
The chromatids still contain the same genes but now have a differnt combination of alleles
What 2 main events happen during meiosis that lead to genetic variation
1) crossing over of chromatids
2) independent segregation of chromosomes
How does crossing over of chromatids lead to genetic variation
Each of the four daughter cells formed form meiosis contain chromatids with differnt alleles
How independent segregation of chromosomes leaded to genetic variation
Each homologous pair of chromosomes in your cells is made up of one chromosome for, your mum (maternal) and one form your dad ( paternal )
When the homologous pairs are separated in meiosis, it’s completly random which chromosome form each pair ends up in which daughter cell
So the 4 daughter cells produced by meiosis have completely differnt combinations of those paternal and maternal chromosomes
This shuffling of the chronometer leads to genetic variation of any potential offspring
Outcomes of mitosis
Produced cells with the same number of chromosomes as the parent cell
Daughter cells are genetically identical to each other and to the parent
2 daughter cells
Outcomes of meiosis
Produced cells with half the number of chronometer as the parents cell
Daughter cells are genetically differnt form one another and the parent cells
Produced 4 daughter cells
My do mitosis and meiosis have differnt outcomes
Mitosis only involves one division which separates the sister chromatids, whereas meiosis has two divisions, which separate the homologous pairs, and then the sister chromatids. There’s no pairing or separating of homologous chromosomes in mitosis, and so no crossing over ot independent segregation of chromosomes.
In humans
How many chromosomes do the daughter cells have after meiosis
23
What is it called when something goes wrong in meiosis and the cell produced contains a variation in the number of whole chromosomes or parts of chromosomes
Chromosome mutation
Caused by errors during meiosis
What does chromosome mutations lead to
Inherited conditions because the errors are Present in the gametes
What is non disjunction
Failure of the chromates to separate properly
What does non-disjunction of chromosomes 21 during meiosis lead to
Down syndrome
What is Down syndrome caused by
A person having an extra copy of chromosome 21
Non disjunction means that chromosome 21 fails to seperate properly during meiosis so one cell gets an extra copy of 21 and another gets none
When the gamete with the extra copy fuses to another gamete at fertilisation, the resulting zygote will have 3 copies of chromosomes 21
What do gene mutations involve
A Changw in the DNA base sequence of chromosomes
What two types of gene mutations are there
Substitution
Deletion
What is substitution mutation
One bass is substituted with another
What is a deletion mutation
One base is deleted
What does a mutation in a gene chase
order of DNA bases Change
So amino acid changes
So the sequnce if amino acid changes
So the protein coded for could be altered
Why do not all mutations affect the offer of amino acids
The degenerate nature of the genetic code means that some amino acids are coded for by more than one DNA triplet
This means that not all substitutions will result in a change to the amino acid sequence of the protein
some substitution will still change for the same amino acid
Will substitution mutation always leads to changed in the amino acid sequence
No
Will deletion mutation always leads to changed in the amino acid sequence
Yes