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B13a) REPRODUCTION

Sexual and asexual reproduction

Reproduction advantages/disadvantages

Sexual

Asexual

Needs two parents.

Only one parent needed (quicker).

Produces variation in the offspring.

Identical offspring (no variation).

If the environment changes variation gives a survival advantage by natural selection.

Vulnerable to rapidly changing conditions due to lack of variation.

Negative mutations are not always inherited.

Negative mutation can affect all offspring.

Natural selection can by speeded up using selective breeding to increase food production.

Food/medicine production can be extremely quick.

Meiosis leads to non-identical cells being formed while mitosis leads to identical cells being formed

Sexual reproduction involves the fusion of male and female gametes.

Sperm and egg in animals.

Produced by meiosis. There is mixing of genetic information which leads to a variety in the offspring.

Pollen and egg cells in flowering plants.

Asexual reproduction involves only one parent and no fusion of gametes.

e.g. cloning of females only in an aphid population.

Only mitosis is involved. There is no mixing of genetic information. This leads to genetically identical clones.

Meiosis halves the number of chromosomes

Gametes are made in reproductive organs (in animals ovaries and testes)

Cells divide by meiosis to form gametes

Copies of the genetic information are made.

The cell divides twice to form four gametes each with single set of chromosomes.

All gametes are genetically different from each other.

Gametes join at fertilisation to restore the number of chromosomes

The new cell divides by mitosis. The number of cells increase. As the embryo develops cells differentiate.

Meiosis

Advantages and disadvantages of sexual and asexual reproduction (Biology only)

Some organisms use both methods depending on the circumstances

Malarial parasites

Asexually in the human host but sexually in a mosquito.

Fungi

Asexually by spores, sexually to give variation.

Plants

Produce seeds sexually, asexually by runners in strawberry plants, bulbs division in daffodils.

DNA and the genome

DNA structure

Polymer made up of two strands forming a double helix.

Contained in structures called chromosomes. A gene is a small section of DNA on a chromosome. Each gene codes for a sequence of amino acids to make a specific protein.

Genetic material in the nucleus is composed of a chemical called DNA.

The genome is the entire genetic material of an organism.

The whole human genome has now been studied.

It is of great importance for future medical developments

Searching for genes linked to different types of disease.

Understanding and treatment of inherited disorders.

Tracing migration patterns from the past.

DNA structure (Biology only)

Phosphate and sugar back bone

phosphate

group

ribose

sugar

base

nucleotide

DNA is polymer made from four different nucleotides. Each nucleotide consists of a common sugar, phosphate group and one of 4 different bases A, C, G & T

Repeating nucleotide units.

A sequence of 3 bases is the code for a particular amino acid. The order of bases controls the order in which each amino acid is assemble to produce a specific protein.

Protein synthesis (HT only)

Mutations occur continuously (HT only)

In DNA the complementary strands C, A, T, G always link in the same way. C always linked to G on the opposite strand and A to T.

(HT) Making new proteins (protein synthesis)

Composed of chains of amino acids. A sequence of 3 bases codes for a particular amino acid.

DNA in the nucleus unravels.

Enzymes make a copy of the DNA strand called mRNA.

mRNA moves from the nucleus to ribosome in the cytoplasm.

Ribosomes translate each 3 bases into amino acids according to mRNA template

Ribosomes link amino acids brought by carrier proteins.

A long chain of amino acids form. Their specific order forms a specific protein.

When the protein chain is complete it folds to form a unique shape. This allows proteins to do their job as enzymes, hormones or new structures such as collagen.

Most do not alter the protein so that its appearance or function is not changed.

Some change the shape and affect the function of proteins e.g. and enzyme active site will change or a structural protein loses its strength

(HT only) Not all parts code for proteins. Non-coding parts can switch genes on and off. Mutations may affect how genes are expressed.

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B13b) REPRODUCTION

(INHERITANCE)

Genetic inheritance

Define terms linked to genetics

Gamete

Sex cells produced in meiosis.

Chromosome

A long chain of DNA found in the nucleus.

Gene

Small section of DNA that codes for a particular protein.

Allele

Alternate forms of the same gene.

Dominant

A type of allele – always expressed if only one copy present and when paired with a recessive allele.

Recessive

A type of allele – only expressed when paired with another recessive allele.

Homozygous

Pair of the same alleles, dominant or recessive.

Heterozygous

Two different alleles are present 1 dominant and 1 recessive.

Genotype

Alleles that are present for a particular feature e.g. Bb or bb

Phenotype

Physical expression of an allele combination e.g. black fur, blonde hair, blue eyes.

The alleles present, or genotype operate at a molecular level to develop characteristics that can be expressed as a phenotype.

Most characteristics are as a result of multiple genes interacting.

Some characteristics are controlled by a single gene e.g. fur colour, colour blindness.

The concept of probability in predicting results of a single gene cross.

Dominant and recessive allele combinations

Dominant

Recessive

Represented by a capital letter e.g. B.

Represented by a lower case letter e.g. b.

3 possible combinations:

Homozygous dominant BB

Heterozygous dominant Bb

Homozygous recessive bb

Using a punnet square (using mouse fur colour as an example)

Parent phenotype

Black fur

White fur

Parent genotype

BB

bb

What gametes are present

In each egg

In each sperm

B

B

The probability of black fur offspring phenotype is 100%. All offspring genotypes are heterozygous (Bb).

Crossing two heterozygous mice (Bb)

The probability of black fur is 75% and white fur 25%. The ratio of black to white mice is 3:1

Sex determination

One pair of chromosomes carry the genes that determine sex

Female

Male

XX

XY

Ordinary human body cells contain 23 pairs of chromosomes

The probability of a male of female child is 50%. The ratio is 1:1

Inherited disorders

Some disorders are inherited. They are caused by the inheritance of certain alleles

Polydactyly

Cystic fibrosis

Caused by inheriting a dominant allele.

Caused by inheriting a recessive allele (both parents have to at least carry it).

Causes a person/animal to have extra toes or fingers.

A disorder of the cell membrane. Patients cannot control the viscosity of their mucus.

Embryo screening and gene therapy may alleviate suffering

Embryo screening/gene therapy

issues

Economic

Costly and not 100% reliable.

Social

Not available to everyone (due to cost).

Ethical

Should only ‘healthy’ embryos be implanted following screening.

Embryo screening: small piece of developing placenta removed to check for presence of faulty genes

Gene therapy: replacing the faulty allele in somatic cells with a normal allele

Using a family tree: If the father was homozygous dominant then all of the offspring would have the disorder. He must be heterozygous

Variation

The genome and its interaction with the environment influence the development of phenotypes

Variation: difference in the characteristics of individuals in a population may be due to

Genetic causes (inheritance)

There is usually extensive genetic variation within the population of a species e.g. hair colour, skin colour, height that can also be affected by environment e.g. nutrition, sunlight.

Environmental causes (condition they have developed in)

A combination of genes and environment

All genetic variation arises in mutation, most have no effect on phenotype, some influence but very few determine phenotype.

Very rarely a mutation will lead to a new phenotype which if is suited to environmental change can lead to rapid change in the species.

Mutations occur continuously