19 — inheritance Flashcards
Inheritance
Refers to the transmission of traits from one generation to another
Gene
A gene is a sequence of DNA nucleotides that controls the formation of a single polypeptide. It s also a unit of inheritance.
Alleles
The one of the different forms of the same gene are called alleles. Alleles of the same gene occupy the same relative positions or gene loci on a pair of homologous chromosomes. Alleles of the same gene have different expressions of the same trait.
Homologous chromosomes [2]
Homologous chromosomes are chromosomes which exist in pairs. Each pair have the same length, size and shape. [1] They have exactly the same sequence of genes, same centromere position and same position of gene loci. [1]
Dominant allele
The allele which expresses itself in the phenotype in both homozygous and heterozygous conditions.
Genotype
The genetic make-up, a combination of alleles for a particular gene of an organism.
Phenotype
The expressed trait in an organism which is influenced by its genotype and the environment.
Homozygous
Homozygous refers to an organism having two identical alleles of a particular gene for a particular phenotype (e.g. DD or dd).
Heterozygous
Heterozygous refers to an organism having two different alleles of a particular gene for a particular phenotype (e.g. Dd).
Recessive allele
A recessive allele is an allele that only expresses itself in the phenotype in a homozygous recessive genotype as the recessive allele is masked by the dominant allele in a heterozygous genotype.
Codominant trait
Codominant trait is when both alleles are equally expressed in the phenotype in the heterozygous condition.
Codominance
Codominance is a condition where both alleles of a gene controlling a trait express themselves equally in a heterozygous genotype and in the phenotype. [1]
For instance, in blood grouping, individuals with IAIB alleles will have both alleles equally expressed and have both antigen A and antigen B on the red blood cells and have the blood group AB. [1]
Define multiple alleles [1]
Alleles of the same gene or locus that has more
than two alleles for a trait. [1]
Mutation [2]
Mutation is a sudden, random, spontaneous change in the structure of a gene where the sequence of nucleotides in the DNA is changed; [1] or a change in the chromosome number. [1]
Down syndrome
3 copies of chromosome 21
A chromosome mutation
Mutagens
Mutagens are agents in the environment that increase the rate
of mutation in an organism.
Examples:
* Ionising radiation
* Certain chemicals
Variation
Variation refers to the differences in a particular trait between individuals of the same species.
Differences betw discontinuous variation and continuous variation
- DV: involves a few clear-cut, distinct phenotypes with no intermediate forms
CV: involves a range of phenotypes
2
DV: controlled by 1 or a few genes
CV: controlled by many genes
- DV: genes do not show additive effect
CV: genes show additive effect
4.
DV: relatively unaffected by env conditions
CV: greatly affected by env conditions
Examples:
CV: skin colour, height
DV: blood group, gender, eye colour
Causes of variation
Variations in organisms may arise due to:
* crossing over and independent assortment of chromosomes and
during meiosis
* mutation in genetic material
* random fertilization of sperm and ovum
Natural selection
Natural selection refers to a process in nature which best-adapted organisms in a population with desirable genes and characteristics survive and pass on their genes to their offspring in the next generation.
Evolution
The gradual change in the inheritable characteristics of a population over time is called evolution.
Explain why observed ratios often differ from expected ratios, especially when there are small numbers of progeny [2]
Observed ratio differs from expected ratio of 3:1 because of small sample size [1] and the random nature of fertilisation from the random fusion of nuclei of gametes, which genotype of each offspring is based on probability. [1]
To obtain an expected ratio of 3:1 in the offspring generation, both parents must be heterozygous for a trait.
To obtain an expected ratio of 1:1 in the offspring generation, 1 parent must be heterozygous while the other is homozygous recessive.
Describe the determination of sex in humans
During fertilisation, an egg will contribute a X chromosome while a sperm will contribute a X or Y chromosome. The female’s ovum can only have one copy of X chromosome, while the male’s sperm can either have a copy of X or Y chromosome. Hence the male gamete determines the sex of a child.
Humans have 22 pairs of autosomes and 1 pair of sex chromosomes.
Sickle cell anaemia gene mutation
- Gene that codes for normal haemoglobin is mutated to form abnormal haemoglobin.
- Abnormal haemoglobin causes the RBCs to be sickle shaped.
- Sickle shaped RBCs carry less oxygen around the body
- Homozygous recessive dies young, heterozygous survives in malaria prone areas
- Heterozygous carry one mutated allele known as carriers.