OCR GCSE Biology B (Twenty First Century)
OCR GCSE Biology B B1.2 How is genetic information inherited? Exam Questions
Free OCR GCSE Biology B exam questions for B1.2 How is genetic information inherited?, with a mark scheme for every pack. Covers sexual reproduction, gametes, meiosis, alleles, dominant and recessive, genetic crosses, Punnett squares, sex determination and family trees.
B1.2 How is genetic information inherited? exam questions
2 question packs of real past exam questions, each with its mark scheme. Do not stop after a few: answer as many as you can without notes, then mark every answer with the mark scheme. The more questions you do, the more quickly you will spot how examiners ask about each idea.
About OCR GCSE Biology B B1.2 How is genetic information inherited?
B1.2 explains how genetic information passes from parents to offspring. You need to describe how gametes are made by meiosis, use the terms allele, dominant, recessive, homozygous and heterozygous correctly, and draw genetic diagrams to predict the outcomes of crosses. Sex determination by the X and Y chromosomes is included. The topic builds on the genome ideas in B1.1 and leads into genetic testing in B1.3 and variation in B6. Examiners regularly ask for Punnett squares, interpretation of family trees and ratios or probabilities, and they reward precise use of genetic vocabulary.
What you need to know
- Gametes and fertilisation Gametes (sperm and egg cells in animals, pollen and egg cells in plants) contain one set of chromosomes. Fertilisation fuses two gametes to give a zygote with paired chromosomes.
- Meiosis Meiosis is a cell division that produces four genetically different gametes, each with half the number of chromosomes of the parent cell. This creates variation in offspring.
- Alleles Alleles are different versions of the same gene. A dominant allele is expressed if one copy is present; a recessive allele is expressed only if two copies are present.
- Homozygous and heterozygous Homozygous means two identical alleles (e.g. AA or aa); heterozygous means two different alleles (Aa). A heterozygous person with a recessive disorder allele is a carrier.
- Genetic crosses Punnett squares predict the probability of offspring genotypes and phenotypes. A cross between two heterozygotes (Aa x Aa) gives a 3 : 1 ratio of dominant to recessive phenotypes.
- Sex determination Human females are XX and males are XY. Every egg carries an X, half of sperm carry X and half carry Y, so each pregnancy has a 50% chance of a boy.
- Single genes and many genes A few characteristics, such as cystic fibrosis, are controlled by a single gene, but most, such as height, are controlled by many genes plus environmental factors.
Common mistakes in B1.2 How is genetic information inherited?
- Treating a predicted ratio as a guaranteed outcome. A 3 : 1 ratio gives probabilities for each child, so actual families can differ.
- Saying dominant alleles are more common. Dominance describes expression, not how often an allele occurs in a population.
- Drawing Punnett squares without showing parental gametes. Show the parent genotypes, the gametes and then the offspring to gain all the marks.
- Confusing meiosis and mitosis. Meiosis makes four genetically different gametes with half the chromosomes; mitosis makes two identical body cells.
- Writing that males decide sex because they are stronger or similar. The sperm decides sex because it carries either an X or a Y chromosome.
Try three B1.2 How is genetic information inherited? exam-style questions
1. State what is meant by the term heterozygous. (1 mark)
Show the mark scheme answer
Having two different alleles of a gene.
2. Cystic fibrosis is caused by a recessive allele, f. Two carriers have a child. Use a genetic diagram to find the probability that the child has cystic fibrosis. (3 marks)
Show the mark scheme answer
Parents are Ff and Ff; gametes F, f and F, f; offspring FF, Ff, Ff, ff; probability of ff is 1 in 4 (0.25 or 25%).
3. Explain why meiosis is important in sexual reproduction. (3 marks)
Show the mark scheme answer
It halves the chromosome number in gametes; so the normal chromosome number is restored at fertilisation; it produces genetically different gametes, increasing variation.
B1.2 How is genetic information inherited? FAQs
What does OCR GCSE Biology B B1.2 cover?
It covers gametes, meiosis, alleles, dominant and recessive inheritance, genetic crosses and how sex is determined by X and Y chromosomes.
Which paper is B1.2 examined in?
J257 has two papers at each tier, Breadth in Biology and Depth in Biology, and content from any chapter, including B1, can be assessed on either one. Expect it to be linked to ideas about science and to other chapters.
How do I get full marks on genetic cross questions?
Use a key for your allele symbols, write parent genotypes and gametes clearly, complete a Punnett square, and finish with the ratio or probability the question asks for.