Higher: B6 - Inheritance, variation and evolution Flashcards
What is DNA and where is it found?
DNA found within chromosomes in the nucleus, is the chemical a cell’s genetic information is composed from.
DNA is a polymer, made up of two strands forming a double helix.
What is a gene?
A small section of DNA on a chromosome. Each gene codes for a particular sequence of which codes for a protein.
What are chromosomes?
Folded up strands of DNA.
Describe how genetic information is arranged and where it is found.
An organism is composed of many cells, each containing a nucleus. Within this are 23 homologous pairs of chromosomes (in humans, excluding gametes), made of coiled DNA. Arranged along chromosomes are small sections of DNA called genes.
Define “genome”.
The entire set of genetic material in an organism.
Why is it important that scientists now understand the human genome?
It allows us to:
- search for genes linked to different types of disease.
- understand and treat inherited disorders.
- trace human migration patterns from the past.
What are mutations?
Random alterations in DNA which occur continuously. They change the sequence of bases in a gene, producing a genetic variant of a protein.
What is sexual reproduction?
A process which involves the fusion of male and female gametes. The mixing of the 2 parents’ genes means offspring are genetically different to their parents, causing variation.
Give 2 types of sexual reproduction.
- Sperm and egg cells in animals.
- Pollen and egg cells in flowering plants.
What is asexual reproduction?
A process which involves only one parent and no fusion of gametes; only mitosis is involved. There is no mixing of genetic information, so offspring are genetically identical, with no variation (clones).
Give 2 advantages of sexual reproduction.
- Produces variation in the offspring which, if the environment changes, gives a survival advantage by natural selection
- It means natural selection can be sped up by humans in selective breeding to increase food production.
Give 3 advantages of asexual reproduction.
- Only one parent needed, making it more time and energy efficient as it doesn’t need to find a mate.
- Faster than sexual reproduction.
- Many identical offspring can be produced when conditions are favourable.
What is meiosis and where does it occur?
The process by which cells in reproductive organs divide to form gametes, which have half the number of chromosomes as somatic (body) cells.
How many chromosomes do human gametes have and why?
In a human, 23, so that, when they fuse with the other sex’s gamete during fertilisation, the product has the full number of 46 chromosomes (like regular somatic cells).
Describe what happens during meiosis.
- The cell duplicates its genetic information.
- The cell divides twice to form 4 gametes, each with a single set of chromosomes.
- All the gametes are genetically different from each other.
What happens during and after the fusion of gametes in fertilisation?
Gametes join at fertilisation to restore the normal number of chromosomes. The new cell divides by mitosis and the number of cells increases. As the embryo develops, cells differentiate.
What are gametes? Name the female and male gametes.
An organism’s reproductive (sex) cells, which are haploid (each cell carries only one copy of each chromosome). Female gametes are ova / egg cells, and male gametes are sperm.
How many pairs of chromosomes do ordinary human body cells contain?
23.
Ordinary human body cells contain 23 pairs of chromosomes. What role do they play?
22 pairs control characteristics only, but the 23rd pair carries the genes that determine sex.
The 23rd pair of chromosomes in human somatic cells carries the genes that determine sex. What are the sex chromosomes in males and females?
- In females, the sex chromosomes are XX.
- In males, the chromosomes are XY.
What is an allele?
A variant form of a gene. There are two alleles for each gene, each on one of a homologous pair of chromosomes.
Compare dominant and recessive alleles.
Each trait is controlled by two alleles, one on each of a homologous pair of chromosomes. The combination of alleles determines the trait expressed:
A dominant allele is always expressed, even if only one copy is present (DD or Dd).
A recessive allele is only expressed if two copies are present (and therefore no dominant allele is present - so only dd).
Define heterozygous and homozygous.
Homozygous = a particular gene that has identical alleles on both homologous chromosomes (both alleles present in an organism for one trait are the same).
Heterozygous = a particular gene that has a different allele on each homologous chromosome (the alleles present in an organism for one trait are the different).
Define “genotype” and “phenotype”.
Genotype = the set of genes in an organism’s DNA which is responsible for a particular trait. Phenotype = the physical expression, or characteristics, of that trait.
Although most phenotypic features are the result of multiple genes interacting, some characteristics are controlled by a single gene. Give 2 examples of this.
Fur colour in mice and red-green colour blindness in humans.
Explain how an organism’s genotype is related to its phenotype.
The alleles present in an organism, or genotype, operate at a molecular level to determine its characteristics that are expressed as a phenotype.