3.2Reproduction and Inheritance
Inheritance — Edexcel Linear - OL Revision Notes & Topical Questions
20 min read 29 parts Lesson 5 of 5 1 quiz
The Genome, DNA, RNA and Protein Synthesis — EDEXCEL LINEAR - OL notes: Describe the structure of DNA and RNA and explain how a gene is transcribed and translated into a protein.The entirety of an organism's DNA is its genome.
- chromosomes
- double helix
- complementary base pairing
- uracil (U) replaces thymine
- single-stranded
- Transcription
Section 1 of 29Genome, genes and chromosomes
The entirety of an organism's DNA is its genome. A gene is a section of a DNA molecule that codes for a particular sequence of amino acids, and these sequences form proteins. Genes control our characteristics because proteins do important jobs in cells: structural proteins such as collagen in skin, enzymes and hormones.
In the nucleus the DNA double helix supercoils to form chromosomes, which are only visible during cell division.
Section 2 of 29DNA structure
DNA (deoxyribonucleic acid) is the genetic material in the nucleus.
Section 3 of 29RNA structure
RNA (ribonucleic acid) is also a polynucleotide, a long chain of nucleotides.
- which brings amino acids during protein synthesis; and ribosomal RNA (rRNA),
- which forms part of ribosomes.
| Feature | DNA | RNA |
|---|---|---|
| Strands | Two (double helix) | One |
| Base replacing T | Thymine | Uracil |
| Sugar | Deoxyribose | Ribose |
Section 4 of 29Transcription and translation
Turning a gene into a protein has two stages.
Transcription (in the nucleus):
Translation (in the cytoplasm, on ribosomes):
- The finished chain is folded and modified into a protein such as an enzyme or antibody.
Alleles are alternative forms of the same gene; they differ slightly in base sequence, which is why they produce different versions of a characteristic.
Section 5 of 29Worked examples
Name the base that pairs with adenine in DNA and the base that pairs with adenine in mRNA. [2]2 marks
In DNA adenine pairs with thymine; when mRNA is made, adenine on the template pairs with uracil.
A DNA template strand reads TACGGT. Give the mRNA sequence made from it. [2]2 marks
Complementary bases: A pairs with T, U with A, G with C, C with G, so mRNA is AUGCCA.
Describe the role of tRNA in translation. [3]3 marks
tRNA has an anticodon that pairs with a codon on mRNA and carries a specific amino acid. It delivers amino acids to the ribosome in the order set by the mRNA so a polypeptide is built.
State two differences between DNA and RNA. [2]2 marks
RNA is single-stranded whereas DNA has two strands; RNA has uracil instead of thymine.
Section 6 of 29Alleles, genotype and phenotype
Alleles are different forms of the same gene, with small differences in base sequence.
The phenotype is the observable characteristic.
| Genotype | Description | Phenotype |
|---|---|---|
| TT | Homozygous dominant | Taster |
| Tt | Heterozygous | Taster |
| tt | Homozygous recessive | Non-taster |
You do not have to memorise PTC. In exams you will be given an unfamiliar characteristic: use capital and lower-case letters for the alleles and always state the phenotype that matches the genotype.
Section 7 of 29Codominance
In codominance both alleles are expressed in the phenotype. Human ABO blood group is an example, with three alleles of one gene: IA, IB and IO. IA makes antigen A and IB makes antigen B; they are codominant with each other but both are dominant to IO, which makes no antigen.
| Genotype | Blood group |
|---|---|
| IAIA or IAIO | A |
| IBIB or IBIO | B |
| IAIB | AB |
| IOIO | O |
Worked idea
- a group A parent and a group B parent can have a group O child only if they are IAIO and IBIO, since the child must inherit IO from each.
- Their Punnett square gives a 25% chance of group O (and 25% each of A, B and AB).
Section 8 of 29Polygenic inheritance
Most characteristics result from several genes interacting, not one gene.
- and you are not expected to explain it with a diagram, only to know that many genes can control one characteristic.
Section 9 of 29Monohybrid inheritance and Punnett squares
Monohybrid inheritance is the inheritance of a characteristic controlled by a single gene. A Punnett square shows the possible allele combinations in offspring, from which you can work out ratios and percentage chances.
Example
- in pea plants the tall allele T is dominant to the short allele t.
- Crossing a pure-breeding tall plant (TT) with a short plant (tt) gives offspring that are all Tt and all tall (the F1 generation).
- Letters for alleles should make it clear which is dominant.
Section 10 of 29Worked examples
A taster (Tt) has children with a non-taster (tt). State the possible genotypes of the children. [2]2 marks
Tt and tt, in the ratio 1:1.
A man with blood group AB and a woman with group O have a child. State the possible blood groups. [3]3 marks
AB parent gametes: IA or IB; O parent: IO. Children are IAIO (group A) or IBIO (group B). Group AB and O are not possible.
Explain what is meant by a heterozygous genotype. [1]1 mark
The two alleles of the gene are different, for example Tt.
Why can height not be shown in a simple Punnett square? [2]2 marks
Height is polygenic, controlled by several genes, so many allele combinations are possible and give a range of phenotypes.
Section 11 of 29F1 and F2 crosses in pea plants
In pea plants the tall allele T is dominant and short t is recessive.
| T | t | |
|---|---|---|
| T | TT | Tt |
| t | Tt | tt |
A cross between a heterozygous tall plant (Tt) and a short plant (tt) gives offspring Tt, Tt, tt, tt: a 1:1 ratio of tall to short. This is a useful test cross.
Section 12 of 29Probabilities from Punnett squares
A Punnett square shows possible allele combinations and their ratio, and the ratio can be converted to probabilities.
Section 13 of 29Family pedigrees
A pedigree diagram traces a characteristic, usually a genetic disorder, through the generations of a family and helps to work out the probability that someone inherits it.
- and whether unaffected parents have affected children.
- (which suggests a recessive allele)
Section 14 of 29Sex chromosomes and inheritance of sex
Sex is determined by one whole chromosome pair, not by one or a few genes.
| X (mother) | X (mother) | |
|---|---|---|
| X (father) | XX | XX |
| Y (father) | XY | XY |
Section 15 of 29Mitosis
Mitosis is nuclear division giving rise to genetically identical cells. Most body cells are diploid, with two copies of each chromosome. Before dividing the chromosomes duplicate (forming X-shaped chromosomes), so after the cell divides each new cell still has two copies of every chromosome.
All body cells except gametes come from mitosis of the zygote. It is used for growth (new cells, for example when a zygote becomes an embryo), repair of damaged tissue, replacement of cells such as skin and red blood cells, and asexual reproduction, where the offspring are genetically identical to the parent.
Section 16 of 29Worked examples
Two heterozygous tall pea plants are crossed. What is the probability of a short offspring? [3]3 marks
Tt x Tt gives TT, Tt, Tt, tt. One in four is short, so the probability is 25% (1/4).
A heterozygous plant is crossed with a short plant. Give the ratio of phenotypes. [2]2 marks
Tt x tt gives Tt, Tt, tt, tt, so 1 tall : 1 short.
Explain why the father determines the sex of a baby. [2]2 marks
The mother can only pass on an X chromosome, while the father produces sperm with either X or Y. Whether the sperm carrying X or Y fertilises the egg decides if the child is XX (girl) or XY (boy).
State three uses of mitosis in humans. [3]3 marks
Growth, repair of damaged tissues, and replacement of cells (also asexual reproduction in other organisms).
Section 17 of 29Meiosis and haploid gametes
Meiosis is a type of nuclear division that gives cells that are genetically different.
Section 18 of 29Mitosis compared with meiosis
| Feature | Mitosis | Meiosis |
|---|---|---|
| Divisions | One | Two |
| Cells produced | Two | Four |
| Chromosome number | Stays the same (diploid) | Halved (haploid) |
| Genetic make-up | Identical to parent cell | Genetically different |
| Where / why | Growth, repair, asexual reproduction | Making gametes in the reproductive organs |
Exam tip
- learn two or three differences and be specific;
- know the reason for each type of division and the cells where it happens.
Section 19 of 29Diploid and haploid cells, random fertilisation
A diploid cell contains two complete sets of chromosomes (2n).
Section 20 of 29Causes of variation
Variation means differences between individuals of the same species.
Section 21 of 29Mutations
Mutations are rare, random changes in the sequence of bases in a gene or chromosome.
Section 22 of 29Worked examples
State two differences between mitosis and meiosis. [2]2 marks
Mitosis produces two genetically identical diploid cells; meiosis produces four genetically different haploid cells.
A human cell divides by meiosis. State the number of chromosomes in each daughter cell and explain why. [2]2 marks
23. Meiosis halves the chromosome number so that fertilisation restores 46.
Explain why a substitution mutation often has less effect than an insertion. [3]3 marks
A substitution changes one base, so only one amino acid changes. An insertion shifts the reading of all later triplets, changing many amino acids.
Identical twins raised apart differ in height. Explain. [2]2 marks
They have the same genes, so the difference is caused by environmental factors such as diet.
Section 23 of 29Effects of mutations
Most mutations do not alter the protein, or alter it so slightly that its function is not changed, so most have no effect on the phenotype.
- so no enzyme-substrate complex forms.
Occasionally a mutation creates a new allele and a new phenotype.
Worked reasoningsuppose a mutation replaces one base in the gene for an enzyme.
Section 24 of 29Causes of mutations
Mutations occur spontaneously and continuously, but the rate increases with exposure to ionising radiation (gamma rays, X-rays and ultraviolet rays), which damages bonds and changes base sequences, and to chemical mutagens such as tar in tobacco smoke. A higher mutation rate can make cells cancerous, which is why these agents are linked with cancers.
Section 25 of 29Darwin's theory of evolution by natural selection
Charles Darwin proposed that evolution has occurred and that natural selection is the process that drives it. The stages are:
Examples are snail shell colour and peppered moth colour. Exam questions often give an unfamiliar example, so learn these four steps and apply them to whatever organism is described.
Key idea
- natural selection acts on variation that already exists.
- Individuals do not change their genes because they need to;
- mutation creates new alleles at random and the environment then selects.
- Natural selection can be contrasted with selective breeding, where humans choose which individuals reproduce.
Section 26 of 29Antibiotic resistance
Natural selection can produce bacteria that are resistant to antibiotics.
A resistant population can only be treated with a different antibiotic, sometimes several, so resistance makes bacterial infections harder to control. In an exam answer include the natural selection steps: variation (mutation), increased survival, increased reproduction and increased allele frequency.
Section 27 of 29Worked examples
Explain how a mutation in an enzyme gene could stop the enzyme working. [3]3 marks
The mutation can change the amino acid sequence, so the protein folds into a different shape. The active site no longer fits the substrate, so enzyme-substrate complexes cannot form.
State two factors that increase the rate of mutation. [2]2 marks
Ionising radiation such as X-rays, gamma rays or UV, and chemical mutagens such as tar in tobacco smoke.
Explain how a population of bacteria becomes resistant to an antibiotic. [4]4 marks
A random mutation gives resistance in one bacterium. The antibiotic kills non-resistant bacteria, while the resistant one survives and reproduces, passing on the allele. The allele becomes more common over generations.
In a woodland, dark moths survive better on dark trees. Use natural selection to explain why dark moths become common. [4]4 marks
There is variation in moth colour. Dark moths are camouflaged and less likely to be eaten, so more survive and reproduce, passing on the allele for dark colour. Over generations it becomes more frequent.
Section 28 of 29Key terms
| Term | Meaning |
|---|---|
| Genome | All of an organism DNA. |
| Gene | Section of DNA that codes for a protein. |
| Complementary base pairing | A with T, and G with C, in DNA. |
| mRNA | Messenger RNA; a copy of a gene carried from nucleus to ribosome. |
| Transcription | Making mRNA from a DNA gene in the nucleus. |
| Translation | Building a polypeptide at a ribosome using the mRNA code. |
| Codon | Triplet of bases on mRNA coding for an amino acid. |
| Anticodon | Triplet of unpaired bases on tRNA. |
| Term | Meaning |
|---|---|
| Allele | Alternative form of a gene. |
| Genotype | The combination of alleles an organism has. |
| Phenotype | The observable characteristic. |
| Dominant | Allele expressed even when only one copy is present. |
| Recessive | Allele expressed only when two copies are present. |
| Homozygous | Having two identical alleles. |
| Heterozygous | Having two different alleles. |
| Codominance | Both alleles are expressed in the phenotype. |
| Polygenic | Controlled by many genes. |
| Term | Meaning |
|---|---|
| F1 generation | Offspring of the first cross between pure-breeding parents. |
| F2 generation | Offspring produced when F1 individuals breed with each other. |
| Punnett square | Grid showing possible allele combinations in offspring. |
| Pedigree | Family tree tracing a characteristic through generations. |
| Sex chromosomes | X and Y; XX is female, XY is male. |
| Mitosis | Nuclear division that gives genetically identical cells. |
| Diploid | Having two sets of chromosomes in the nucleus. |
| Term | Meaning |
|---|---|
| Meiosis | Division giving four genetically different haploid gametes. |
| Haploid | Having one set of chromosomes (n). |
| Diploid | Having two sets of chromosomes (2n). |
| Variation | Differences between individuals of the same species. |
| Mutation | Random change in DNA base sequence. |
| Insertion | Mutation adding a base. |
| Deletion | Mutation removing a base. |
| Substitution | Mutation swapping one base for another. |
| Term | Meaning |
|---|---|
| Natural selection | Process in which individuals with advantageous alleles survive and reproduce more. |
| Evolution | Change in the inherited characteristics of populations over many generations. |
| Antibiotic resistance | Ability of bacteria to survive an antibiotic, due to a resistance allele. |
| Ionising radiation | X-rays, gamma rays and UV, which can cause mutations. |
| Mutagen | Chemical or radiation that raises the rate of mutation. |
| Allele frequency | How common an allele is in a population. |
Section 29 of 29Exam technique
Marked practiceQuizzes for this lesson
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