Reproduction & Inheritance (Edexcel A Level Biology (A) SNAB): Flashcards

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  • Define gamete.

Cards in this collection (48)

  • Define gamete.

    A gamete is a sex cell, such as a sperm or egg, that fuses with another during fertilisation.

  • Why are gametes haploid?

    They are formed by meiosis and contain only one copy of each chromosome.

    This means fertilisation restores the full (diploid) chromosome number.

  • How many chromosomes does a human gamete contain?

    23 single chromosomes.

  • How is a sperm cell adapted for its function?

    It has a flagellum to swim to the egg.

    It has many mitochondria for energy, and an acrosome of digestive enzymes to penetrate the egg.

  • What is the function of the acrosome in a sperm cell?

    It contains digestive enzymes.

    These break down the protective layer around the egg so the sperm can enter.

  • Why do sperm cells contain many mitochondria?

    To provide energy (ATP) for movement of the flagellum, so the sperm can swim to the egg.

  • Why is an egg cell much larger than a sperm cell?

    Most of its space is filled with food stores.

    These nourish the growing embryo after fertilisation.

  • Define zona pellucida.

    The zona pellucida is the jelly-like glycoprotein layer around the egg cell that hardens after fertilisation to block other sperm.

  • What is the function of the zona pellucida after fertilisation?

    It forms an impenetrable barrier.

    This prevents other sperm nuclei from entering the egg.

  • Gametes are formed by the process of , so they are haploid.

    Gametes are formed by the process of meiosis, so they are haploid.

  • True or False?

    The egg cell has a flagellum to help it move to the sperm.

    False.

    The sperm cell has the flagellum; the egg cell does not move towards the sperm.

  • What is formed when a sperm and egg fuse?

    A zygote — a fertilised egg with the full diploid chromosome number.

  • Define fertilisation.

    Fertilisation is the fusion of the nuclei of a male gamete (sperm) and a female gamete (egg).

  • Where does fertilisation take place in a mammal?

    In the oviduct.

  • How do sperm cells find the egg cell?

    They follow a chemical trail released by the egg.

    They swim up through the cervix and uterus into the oviduct.

  • Define the acrosome reaction.

    The acrosome reaction is the release of digestive enzymes from the sperm head, which digest a path through the egg's protective layer.

  • What is the role of the enzymes released in the acrosome reaction?

    They digest a path through the zona pellucida.

    This allows the sperm to reach and pass through the egg cell membrane.

  • Define the cortical reaction.

    The cortical reaction is the release of cortical granules from the egg, which make the zona pellucida thicken and harden to block other sperm.

  • Why is the cortical reaction important?

    It ensures only one sperm fertilises the egg.

    The hardened zona pellucida stops any further sperm entering.

  • What happens immediately after the sperm and egg nuclei fuse?

    A zygote is formed with the full 46 chromosomes.

    Half come from the father and half from the mother.

  • How does a zygote develop into an embryo?

    It divides repeatedly by mitosis.

    The new cells then become specialised to form the body tissues.

  • The cortical reaction causes the zona pellucida to thicken and , preventing other sperm from entering.

    The cortical reaction causes the zona pellucida to thicken and harden, preventing other sperm from entering.

  • True or False?

    The acrosome reaction occurs in the egg cell.

    False.

    The acrosome reaction occurs in the sperm cell; the cortical reaction occurs in the egg.

  • Why does fertilisation restore the diploid chromosome number?

    Each haploid gamete carries 23 chromosomes.

    Their fusion combines two sets, giving the zygote the full 46.

  • Define locus.

    A locus is the specific position of a gene on a chromosome.

  • Why is a gene for a characteristic always found at the same locus?

    Each gene occupies a specific, fixed position on a particular chromosome.

    Different alleles of that gene sit at the same locus.

  • Define autosomal linkage.

    Autosomal linkage is when two or more genes on the same autosome are inherited together, rather than assorting independently.

  • What is an autosome?

    Any chromosome that is not a sex chromosome.

  • Why do linked genes not assort independently?

    They are on the same chromosome.

    So they stay together in their parental combination and are passed on together.

  • Define sex-linked gene.

    A sex-linked gene is one carried on a sex chromosome, so its inheritance depends on the sex of the individual.

  • What are the sex chromosome combinations for males and females?

    Females are XX.

    Males are XY.

  • On which sex chromosome are most sex-linked genes found?

    The X chromosome, which is longer than the Y.

  • Why are males more likely to show sex-linked recessive conditions?

    Males have only one X chromosome, so only one copy of an X-linked gene.

    A single recessive allele is expressed, as there is no second allele to mask it.

  • Give two examples of sex-linked recessive conditions.

    Red-green colour blindness and haemophilia.

  • Genes on the same autosome that are inherited together are said to be .

    Genes on the same autosome that are inherited together are said to be linked.

  • True or False?

    A female can be a carrier of a sex-linked recessive condition without being affected.

    True.

    With two X chromosomes, a dominant allele on one can mask the recessive allele on the other.

  • Define meiosis.

    Meiosis is nuclear division that produces four genetically different haploid gametes from one diploid parent cell.

  • How many divisions and daughter cells does meiosis involve?

    Two divisions (meiosis I and meiosis II).

    They produce four haploid daughter cells.

  • During which division of meiosis does the chromosome number halve?

    Meiosis I, when the homologous pairs are separated.

  • Name the two processes in meiosis that increase genetic variation.

    Crossing over and independent assortment.

  • Define crossing over.

    Crossing over is the exchange of alleles between non-sister chromatids of homologous chromosomes during meiosis I.

  • How does crossing over increase genetic variation?

    Sections of chromatid break and rejoin with the other chromosome.

    This produces new combinations of alleles on the chromosomes.

  • Define chiasma.

    A chiasma is a point where non-sister chromatids cross over and exchange alleles during meiosis.

  • Define independent assortment.

    Independent assortment is the random arrangement of homologous pairs at the equator in meiosis I, giving different allele combinations in the gametes.

  • How does independent assortment increase genetic variation?

    Each homologous pair lines up randomly, independently of the others.

    This produces many different combinations of chromosomes in the gametes.

  • The exchange of alleles between non-sister chromatids in meiosis is called over.

    The exchange of alleles between non-sister chromatids in meiosis is called crossing over.

  • True or False?

    Meiosis produces genetically identical daughter cells.

    False.

    Meiosis produces genetically different cells, because of crossing over and independent assortment.

  • Why is producing genetically different gametes advantageous?

    It increases genetic variation in the offspring.

    This provides the variation that natural selection can act on.

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