3.4 Genetic information, variation and relationships between organisms Flashcards
3.4.1 DNA, genes and chromosomes
What is DNA? (2 points)
DeoxyriboseNucleic Acid
Polynucleotide
Compare Eukaryotic DNA with Prokaryotic DNA (4 points)
Eukaryotic DNA is large and long whereas prokaryotic is smaller and shorter as has less non coding DNA
Eukaryotic DNA is associated with proteins (histones) whereas Prokaryotic is not
Eukaryotic DNA is contained within the nucleus whereas prokaryotic DNA is not and is found free floating in cytoplasm so can mutate and replicate faster
Prokaryotic DNA is a single circular loop whereas eukaryotic found in linear chromosomes
What is a histone? (2 points)
A protein that DNA coils around to make a compact chromosome
Help to support the DNA
What is a chromosome? (1 point)
How DNA is stored in the nucleus
What are the features of chromosomes? (3 points)
23 pairs of chromosomes
Consist of maternal and paternal chromosomes
Cells that contain 23 pairs are diploid as have both sets of chromosomes
What is a homologous pair of chromosomes? (3 points)
Pairs of matching chromosomes
Both chromosomes are the same size and have the same genes, although they could have different alleles
Alleles coding for same characteristic will be found at same fixed position (loci) on each chromosome in homologous pair
What is a gene? (2 points)
A sequence of DNA bases that codes for either a polypeptide or functional RNA
Each gene is found at the same position (loci) on both the maternal and paternal chromosomes
What is an allele? (1 point)
A different version of a gene
What is the locus? (1 point)
The location of the gene on the chromosome
What is the genetic code? (1 point)
The sequence of base triplets (codons) in mRNA which code for a specific amino acid
What are the features of the genetic code? (4 points)
The code is a triplet code – one triplet (3 nucleotide bases) codes for one amino acid
The code is non-overlapping – base triplets don’t share their bases
The code is universal – each triplet code always codes for the same one amino acid
The code is degenerate – some amino acids are coded for by more than one triplet
How many possible triplets and amino acids exist? (2 points)
There are 64 possible triplets and 20 different amino acids
Why don’t all triplet codes result in amino acids? (2 points)
Some act as punctuation marks
Some indicate start and stop points for start/end of an amino acid chain (codons)
3.4.2 DNA and protein synthesis
What is transcription? (2 points)
The first stage of protein synthesis
The process by which pre-mRNA is formed
Describe the process of transcription (9 points)
Hydrogen bonds between two DNA strands in gene break due to DNA helicase, separating strands and DNA molecule uncoils exposing some of the bases
One of the strands is then used as a template to make mRNA copy
RNA polymerase lines up free RNA nucleotides alongside the exposed bases on template strand. Free bases are attracted to exposed bases
Complementary base pairing occurs between RNA nucleotides and DNA bases and are joined by RNA polymerase, forming mRNA molecule
RNA polymerase moves along DNA separating the strands and assembling mRNA strand
Hydrogen bonds between uncoiled strands of DNA reform once RNA polymerase has passed by and strands coil back into a double helix
When RNA polymerase reaches a stop signal, it stops making mRNA and detaches from DNA
mRNA moves out of nucleus through nuclear pore and attaches to ribosome for translation to take place
What happens before mRNA leaves the nucleus? (1 point)
Splicing
- Introns (non-coding pieces of mRNA) are removed and functional exons (code for amino acids) are joined to form mRNA
- When introns included = pre-mRNA
- When introns removed = mRNA
What is translation? (2 points)
The second stage of protein synthesis
Process by which mRNA is used to make a specific polypeptide
Describe the process of translation (8 points)
The mRNA attaches itself to a ribosome and transfer RNA (tRNA) molecules carry amino acids to it. ATP provides energy for bond between amino acid and tRNA molecule to form
A tRNA molecule, with an anticodon that is complementary to the first codon on mRNA, attaches itself to the mRNA by specific base pairing
A second tRNA molecule attaches itself top next codon on mRNA in same way
The two amino acids attached to tRNA molecules are joined by a peptide bond
The first tRNA molecule moves away, leaving its amino acid behind
A third tRNA molecule binds to next codon on mRNA. Its amino acid binds to first two and second tRNA molecule moves away
Process continues producing a chain of linked amino acids (polypeptide chain) until there’s a stop signal on mRNA molecule
Polypeptide chain moves away from ribosome and translation is complete
Polypeptides join to form a protein
Describe the structure of a tRNA molecule (4 points)
tRNA is a single polynucleotide strand folded into a clover shape
Hydrogen bonds between specific base pairs hold the molecule in shape
It has a specific sequence of 3 bases at one end called anticodon
Have amino acid binding site at the other end
Describe the structure of mRNA (1 point)
Is a single polynucleotide strand
3.4.3 Genetic diversity can arise as a result of mutation or during meiosis
What is a mutation? (1 point)
A change in one or more nucleotide base or a change in sequence of bases in DNA
What are the three main ways of a mutation arising? (3 points)
Deletion – A nucleotide is lost from the DNA base sequence
Insertion – A nucleotide is added to the DNA sequence
Substitution – One nucleotide is replaced by another nucleotide with a different base
What effect does deletion and insertion have? (1 point)
Have greatest effect as cause change in whole sequence (frame shift – every amino acid after insertion/deletion will change)
What effect does substitution have? (1 point)
Only effects one amino acid but if degenerate code will have no effect
What is a chromosomal mutation? (1 point)
Changes in the structure or number of whole chromosomes
What are the two main types of chromosomal mutations? (2 points)
Polyploidy – occurs when organisms have 3 or more sets of chromosomes and occurs mainly in plants
Non-disjunction – Chromosomes fail to separate during meiosis
Compare mitosis and meiosis (5 points)
Mitosis produces cells for growth and repair whereas meiosis leads to production of gametes and ensures diversity in reproduction
Mitosis involves 1 cell division whereas meiosis involves 2
Mitosis produces 2 daughter cells whereas meiosis produces 4
In mitosis the daughter cells are diploid (two copies of every chromosome) whereas in meiosis the cells are haploid (only one copy of each)
In mitosis the daughter cells are identical to parent cells whereas in meiosis there is more variation as not identical
What is meiosis? (1 point)
The process by which a diploid nucleus (2n) divides to produce four haploid daughter nuclei (n)
Describe the process of meiosis (9 points)
Interphase - DNA unravels and replicates so there are two copies of each chromosome (chromatids)
Prophase 1 - Nuclear envelope breaks down and chromosomes condense
Metaphase 1 - Spindle fibres form and chromosomes line up along the equator
Anaphase 1 - Homologous chromosomes are pulled apart to opposite poles
Telophase 1 and cytokinesis - Two daughter cells are formed and cytoplasm divides
Prophase 2 - Two diploid daughter cells are produced, and nuclear envelope does not need to break down again
Metaphase 2 - Chromosomes line up along equator and attach to spindle fibres
Anaphase 2 - Sister chromatids are pulled apart to opposite poles
Telophase 2 and cytokinesis - Nuclear envelope reforms and four haploid cells are produced
How does meiosis lead to genetic diversity? (2 points)
Crossing over of chromatids – Crossing over of chromatids in meiosis 1 means that each of four daughter cells formed from meiosis contains chromosomes with different alleles
Independent segregation – Each homologous pair of chromosomes in cells is made up of one maternal chromosome and one paternal chromosome. When homologous pairs are separated in meiosis 1 its random which chromosome from each pair ends up in which daughter cell. So, four daughter cells produced have completely different combinations of maternal and paternal chromosomes which leads to genetic variation in offspring
3.4.4 Genetic diversity and adaptations
What is genetic diversity? (1 point)
The total number of different alleles in a population
How does genetic diversity lead to natural selection? (2 points)
Greater number of different alleles of a species, the greater the genetic diversity. The greater the genetic diversity, the more likely the species can adapt to environmental change which leads to natural selection
What increases genetic diversity? (2 points)
Mutations in the DNA which forms new alleles
Gene Flow - different alleles being introduced into a population when individuals from another population migrate into them and reproduce