Chapter 3.4 Genetic Info & Variation Flashcards
Compare prokaryotic + eukaryotic cells DNAs
prokaryotic
Short
Circular strands
Not associated with proteins
eukaryotic
Very long
Linear strands
Associated with proteins called histones
Apart from nucleus
where else is DNA found in eukaryotic cells
+ describe its structure
In EUKARYOTIC CELLS
Mitochondria & chloroplast contain DNA
+this DNA is short, circular & not associated with proteins (like prokaryotic DNA)
{This DNA can be used to synthesis their own proteins/enzyme that are used inside the organelle itself }
think about the extra reading about how there is a theory that both these organelles where bacteria cells themselves at some point which would explain the need for DNA
Def of gene
A base sequence of DNA that codes for the amino acid sequence of a polypeptide and a functional RNA
Why is the genetic code
1) universal
2) non-overlapping
3) degenerate
-universal= the same triplet (codon) code used by all organism
- Non-overlapping=
-Degenerate= most amino acids code for more than one codon
Def of genome?
The complete set of genes in a cell
Def of proteome
The full range of proteins a cell is able to produce
Compare structures of mRNA & tRNA
mRNA tRNA
-straight chain. - folded into a clover leaf shape
- variable in length. - fixed length (3 bases)
- longer chains. - shorter chains
- doesn’t attach amino acids. - attachment site for amino acids to bind
[- only polypeptide bonds - regions of H bonds within ]
Explain transcription process
Transcription - making an mRNA copy of DNA nucleotide sequence in a gene
1) DNA helicase unzips the DNA molecule
2) Free RNA nucleotides form complementary base pairs with nucleotides from non-sense strand of exposed DNA
3) enzyme RNA polymerase joins RNA nucleotides together using phosphodiester bonds to make mRNA
4) mRNA is a copy of the ‘sense’ strand of DNA (but U replaces T bases)
if prokaryotic then mRNA produced is ready for use in translation at this stage
if eukaryotic the pre-mRNA is then processed
inrons- non coding sections-are removed and
exons- coding sections- get spliced together to from mRNA ready for translation
Explain translation process
Translation- occurs at ribosomes + is when mRNA codons are used to create a sequence of amino acids in a polypeptide chain
1) mRNA binds to ribosome at start codon
2) tRNA molecule’s anticodon binds to each complementary codon on mRNA
3) amino acids carried by tRNA molecules join by peptide bonds to from polypeptide chain
(These peptide bonds are formed using enzyme + ATP which is hydrolysed to provide required energy)
4) final protien is release from ribosome where it can then fold into its final structure
Draw diagram to show structure of tRNA molecule
See notes
Def of anticodon (tRNA)
A triplet of bases complementary to codon on mRNA molecule
Mutation
Change to quantify or structure of DNA of an organism
Gene mutation
Change to one or more nucleotide bases in the DNA of gene/ rearrangement in the sequence of bases of a gene
Types of gene mutations and what they are?
1) substitution
Replacement of 1 nucleotide with a different nucleotide
2) insertion
Addition of 1 or more nucleotides
3) deletion
Loss of one or more nucleotides
4) inversion
A cut portion is inverted 180o then rejoined to the same place within the gene
5) duplication
A whole gene/section is duplicated so that 2 copies of gene/section appear on the same chromosome
6) translocation
The section of the gene is cut off and attached to a separate gene
When can substitutions be harmful or neutral
HARMFUL
- if the replacement nucleotide causes the amino acid to change which leads to an unfunctional or harmful protein.
NEUTRAL
- if the replacements nucleotide is in the non coding region (intron region removed) then no effect will be seen in proteins produced
- if the replacement nucleotide still forms the same protein
Why might a time shift not be formed during insertion or deletion of DNA
-If 3 nucleotides are added or removed
- if the nucleotide is added to the ends
Types of chromosome mutations?
1) POLYPLOIDY (changes in the whole sets of chromosomes)
- organism have 3 or more sets of chromosomes rather that usual 2
mostly occurs in plants
2) HYBRIDS (changes in wholes sets of chromosomes)
- can be formed by combining sets of chromosomes from different species closely related
A new species may arise if the chromosome number of the hybrid is a multiple of the original chromosome number (because meiosis can occur)
mostly occurs in plants
3) NON-DISJUNCTION
- during meiosis
Homologous pairs of chromosomes fail to separate during meiosis
A gamete will have either 1 or more or 1 fewer chromosomes
mostly occurs in plants
Types of chromosome mutations?
1) POLYPLOIDY (changes in the whole sets of chromosomes)
- organism have 3 or more sets of chromosomes rather that usual 2
mostly occurs in plants
2) HYBRIDS (changes in wholes sets of chromosomes)
- can be formed by combining sets of chromosomes from different species closely related
A new species may arise if the chromosome number of the hybrid is a multiple of the original chromosome number (because meiosis can occur)
mostly occurs in plants
3) NON-DISJUNCTION
- during meiosis
Homologous pairs of chromosomes fail to separate during meiosis
A gamete will have either 1 or more or 1 fewer chromosomes
mostly occurs in plants
Def of mutagenic agent
An outside factor that increases the basic mutation rate
Causes of mutations (chromosome/gene)?
-
mutations occur spontaneously
During DNA replication -
mutagenic agents
1) high energy ionising radiation
Can distrust structure of DNA
2) chemicals (NO2 & Benzopyrene)
NO2- disrupt DNA structure interfere with transcription
Benzopyrene - inactivates a tumour supressor gene TP53 leading to cancer
Benzopyrene is found in tobacco smoke & NO2 from burning fossil fuels
define degeneracy and explain its significance in genetic mutation
- 1 or more triple codes can code for the same amino acid
- substitution replacement of bases in the triplet code can code for the same amino acid (silent mutations can arise)
- 3rd bases in triplet most likely to result in scilent mutation
(as which amino acid of the 3rd base in a triplet can have multiple bases & still result in coding for same amino acid)
impacts/outcomes of silent mutations?
silent mutations
- new allele formed but degeneracy means amino acid not affected
- new allele friend in intron that is removed during slicing of mRNA
- new allele doesn’t affect tertiary protein structure (recessive)
*no affect to reproduction/survival
Impacts/outcomes of harmful mutations?
harmful mutations
- new allele formed results in charge in polypeptide that negatively changes the tertiary properties
- may result in decreased survival and reproduction
Impacts/outcomes of beneficial mutations?
beneficial mutations
- new allele is formed resulting in change in polypeptide that positivity changes tertiary properties
- may result in increased survival & reproduction
Difference between haploid and diploid cells
Diploid cells
- contain 2 types of each chromosome (homologous chromosomes)
- produced by mitosis cell division
Haploid cells
- only contins 1 type of each chromosome
- produced via meiosis cell division
Purpose of meiosis
To produce gamates that each contian
1) a haploid number of chromosomes
2) a different combination of alleles (i.e show variation )
Describe + explain the process of crossing over/recombination
+how it leads to genetic variation during meiosis?
During prophase 1 homologous pairs of chromosomes associate (form bivalent )
Chiasmata form (sister chromatids attach)
Lengths of chromatids/alleles are exchanged
Producing new combination of alleles
Describe + explain the process of independent segregation
+how it leads to genetic variation during meiosis?
During metaphase 1, pairs of homologous chromosomes (bivalent)
Line up at equator, each pair line up randomly
This results in gamates that are genetically unique
(Gamates each carry a different combination of maternal &paternal chromosomes)
Def of variation
Name + explain the 3 events in meiosis/sexual reproduction that cause genetic variation
1) independent segregation
- produces gametes with random combination of maternal & paternal chromosomes
2) crossing over
- new combination of alleles produced as portions of sister chromatids are exchanged
3) random fusion of gametes
- produces offspring with unique combination of maternal & paternal alleles