Sexual vs Asexual Reproduction, Genetic Crosses & Inherited Disorders
Organisms pass genetic information to their offspring either through sexual reproduction (involving the fusion of haploid male and female gametes formed by meiosis to create genetically varied offspring) or asexual reproduction (involving mitosis from a single parent to produce genetically identical clones). Single-gene characteristics are controlled by different forms of a gene called alleles, which can be dominant or recessive. Examiners test students' ability to construct Punnett square diagrams, calculate phenotypic ratios and probabilities for inherited disorders (cystic fibrosis and polydactyly), and evaluate the advantages of both sexual and asexual reproduction.
- Sexual vs Asexual Reproduction
- Sexual reproduction involves the fusion of male and female gametes (sperm and egg in animals; pollen and egg cells in flowering plants) formed by meiosis, mixing genetic information and creating variation. Asexual reproduction involves only one parent and cell division by mitosis; there is no fusion of gametes and offspring are genetically identical clones.
- Genotype, Phenotype, Homozygous & Heterozygous
- An allele is an alternative version of a gene. Genotype is the combination of alleles an organism has (e.g., Bb). Phenotype is the observable physical characteristic expressed (e.g., brown eyes). Homozygous means having two identical alleles (BB or bb); heterozygous means having two different alleles (Bb).
- Dominant vs Recessive Alleles
- A dominant allele (represented by a capital letter, e.g., B) is always expressed in the phenotype even if only one copy is present (BB or Bb). A recessive allele (lowercase letter, e.g., b) is only expressed if two copies are present (homozygous recessive, bb) and no dominant allele is present.
Mitosis (2n → 2n) vs Meiosis (2n → n) & Ribosome Protein Synthesis
1. Interphase (DNA Replication)
Diploid parent cell (2n = 46 in humans). DNA replicates so each chromosome consists of two identical sister chromatids; subcellular organelles (mitochondria, ribosomes) also double.
Diploid germ cell (2n = 46). DNA replicates once to form homologous pairs of doubled chromosomes ready for two rounds of division.
Key Concepts & Exam Definitions (6)
- Sexual vs Asexual Reproduction
- Sexual reproduction involves the fusion of male and female gametes (sperm and egg in animals; pollen and egg cells in flowering plants) formed by meiosis, mixing genetic information and creating variation. Asexual reproduction involves only one parent and cell division by mitosis; there is no fusion of gametes and offspring are genetically identical clones.
- Genotype, Phenotype, Homozygous & Heterozygous
- An allele is an alternative version of a gene. Genotype is the combination of alleles an organism has (e.g., Bb). Phenotype is the observable physical characteristic expressed (e.g., brown eyes). Homozygous means having two identical alleles (BB or bb); heterozygous means having two different alleles (Bb).
- Dominant vs Recessive Alleles
- A dominant allele (represented by a capital letter, e.g., B) is always expressed in the phenotype even if only one copy is present (BB or Bb). A recessive allele (lowercase letter, e.g., b) is only expressed if two copies are present (homozygous recessive, bb) and no dominant allele is present.
- Cystic Fibrosis (Recessive Inherited Disorder)
- A genetic disorder of cell membranes caused by a recessive allele (f). Causes the body to produce lots of thick, sticky mucus in the air passages (lungs) and pancreas. An individual must inherit two recessive alleles (ff) to have the disorder; heterozygous individuals (Ff) are symptomless carriers.
- Polydactyly (Dominant Inherited Disorder)
- An inherited condition in which a baby is born with extra fingers or toes, caused by a dominant allele (D). Because the allele is dominant, an individual only needs to inherit one copy of the faulty allele (Dd or DD) from one parent to have polydactyly; it is impossible to be an unaffected carrier.
- Embryo Screening & Gene Therapy Ethics
- Amniocentesis, chorionic villus sampling (CVS), or pre-implantation genetic diagnosis (PGD during IVF) tests embryo DNA for genetic disorders. Advantages: reduces suffering and allows parents to prepare or terminate affected pregnancies. Disadvantages: invasive tests carry a small risk of miscarriage, high cost, and ethical concerns about 'designer babies' or prejudice against disabled individuals.
Quick-Fire Flashcards (6)
Click any card to check the answer, then mark it as Known to track your progress.
Why does meiosis produce four genetically different haploid cells, whereas mitosis produces two genetically identical diploid cells?
If two heterozygous carriers of cystic fibrosis (Ff) have a child, what is the probability the child will have cystic fibrosis?
A man with heterozygous polydactyly (Dd) and an unaffected woman (dd) have a child. What is the probability the child has polydactyly?
Give two advantages of sexual reproduction and two advantages of asexual reproduction.
How do strawberry plants and daffodil bulbs reproduce asexually?
Why is it impossible for two unaffected parents to have a child with polydactyly (unless a new mutation occurs)?
Exam-Style Questions & Mark Schemes (4)
Write or think through your answer first, then click Check Mark Scheme to see the exact points examiners award marks for.
- Q1
Two parents who do not have cystic fibrosis have a first child who is born with cystic fibrosis. Using a genetic cross (with F for the normal allele and f for the cystic fibrosis allele), explain how this happened and state the probability that their second child will also have cystic fibrosis. [5 marks]
Click “Check Mark Scheme” to compare your answer, 1. Cystic fibrosis is caused by a recessive allele (f). Since neither parent has the disorder, but they passed it to their child, both parents must be heterozygous carriers with genotype Ff [1 mark]. 2. Parental gametes: Both mother and father produce gametes containing either F or f [1 mark]. 3. Offspring genotypes from Punnett square (Ff x Ff): FF, Ff, Ff, ff [1 mark]. 4. The first child inherited one recessive allele (f) from each parent, giving the homozygous recessive genotype ff [1 mark]. 5. Every pregnancy is an independent event, so the probability that their second child will also be ff (have cystic fibrosis) is 25% (or 1/4 or 0.25) [1 mark].
- Q2
Compare the advantages of sexual and asexual reproduction for an organism such as the malarial parasite or a strawberry plant that can use both methods. [4 marks]
Click “Check Mark Scheme” to compare your answer, 1. Sexual reproduction mixes alleles from two parents via meiosis and fertilisation, producing genetic variation in the offspring [1 mark]. 2. Genetic variation creates a survival advantage if the environment changes or a disease/drug is introduced, as some individuals may possess beneficial alleles and survive by natural selection [1 mark]. 3. Asexual reproduction requires only one parent (no need to find a mate or pollinator), which saves time and energy [1 mark]. 4. When environmental conditions are already favourable, asexual reproduction allows the organism to produce large numbers of genetically identical, well-adapted offspring very rapidly [1 mark].
- Q3
In a family pedigree chart, a father and daughter both have Huntington's disease (or polydactyly), caused by a dominant allele (D), while the mother and son are unaffected. Determine the exact genotype of all four family members and explain your reasoning. [4 marks]
Click “Check Mark Scheme” to compare your answer, 1. The unaffected mother and unaffected son must both be homozygous recessive (dd), because if they had even one dominant D allele they would show the condition [1 mark]. 2. The affected daughter must have inherited one recessive allele (d) from her unaffected mother (dd) and one dominant allele (D) from her father, so her genotype is heterozygous (Dd) [1 mark]. 3. The affected father passed a recessive allele (d) to his unaffected son (dd) [1 mark]. 4. Therefore, the father cannot be DD; his genotype must also be heterozygous (Dd) [1 mark].
- Q4
Evaluate the use of embryo screening (such as Pre-implantation Genetic Diagnosis during IVF or amniocentesis) for couples with a family history of a severe genetic disorder. [4 marks]
Click “Check Mark Scheme” to compare your answer, 1. Advantage: Screening identifies whether an embryo has the faulty alleles, allowing only healthy embryos to be implanted during IVF, preventing a child from being born with a painful, life-limiting disorder [1 mark]. 2. Advantage: It reduces the emotional stress on families and saves long-term healthcare costs of treating lifelong genetic conditions [1 mark]. 3. Disadvantage: Invasive prenatal screening methods (like amniocentesis) carry a small medical risk of causing a miscarriage of a potentially healthy fetus [1 mark]. 4. Ethical concern: Screening during IVF results in embryos with faulty alleles being destroyed (or pregnancy termination), which some people oppose on religious/moral grounds or fear could lead to 'designer babies' and discrimination against disabled people [1 mark].
Common Exam Questions (4)
What are the advantages of sexual reproduction vs asexual reproduction?
Sexual reproduction produces genetic variation in the offspring; if the environment changes or a new disease emerges, some individuals are likely to have alleles that allow them to survive via natural selection. Asexual reproduction requires only one parent (no need to find a mate), is much faster, uses less energy, and allows rapid colonisation when conditions are favourable.
Which organisms can reproduce both sexually and asexually?
GCSE Biology specifies three key examples: 1. Malarial parasites (reproduce asexually inside the human host, but sexually inside the mosquito vector). 2. Many fungi (reproduce asexually by spores, and sexually to create variation in harsh conditions). 3. Many plants (reproduce sexually via flowers and seeds, and asexually via runners like strawberries or bulbs like daffodils).
What is the difference between cystic fibrosis and polydactyly?
Cystic fibrosis is a disorder of cell membranes (causing thick, sticky mucus in the lungs and pancreas) caused by a recessive allele (ff); therefore, an unaffected person with one copy (Ff) is a carrier. Polydactyly (having extra fingers or toes) is caused by a dominant allele (Dd or DD); therefore, anyone with even one copy of the allele will have the condition, and there are no unaffected carriers.
How are sex chromosomes inherited in humans?
Humans have 23 pairs of chromosomes; 22 pairs control body characteristics, and the 23rd pair determines sex. Females have two X chromosomes (XX), so all egg cells carry an X chromosome. Males have one X and one Y chromosome (XY), so 50% of sperm carry X and 50% carry Y. Every pregnancy has a 50% (0.5 or 1:1) probability of producing a boy or a girl.
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Related study guides
DNA, Genes & Inheritance
DNA (deoxyribonucleic acid) stores the genetic instructions needed for an organism to grow, develop, and reproduce. Packaged into chromosomes inside the cell nucleus, genes code for specific proteins, while inherited combinations of alleles determine an organism's genotype and observable characteristics (phenotype).
Mitosis vs Meiosis
Mitosis and meiosis are the two types of nuclear division in eukaryotic cells. Mitosis involves 1 division that produces 2 genetically identical diploid daughter cells for growth and tissue repair, whereas meiosis involves 2 divisions (meiosis I and II) that produce 4 genetically distinct haploid gametes for sexual reproduction.
Selective Breeding, Genetic Engineering & Cloning
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