6.20 - Patterns of inheritance Flashcards
Chlorosis
- where a plants leaves look pale or yellow
- occurs because not enough chlorophyll is being produced
Mostly due to environmental factors (variation): - mineral deficiencies (iron and magnesium)
- lack of light
- viral infections (TMV affects cell metabolism)
Even though genetic factors in a plant are likely to code for green leaves, the environment plays a key role in the final leaf appearance/phenotype
Animal body mass
- determined by a combination of genetic (mutation or variation in fat storage) and environmental factors
- dramatic variations are usually a result of environmental factors (calorific intake, exercise, disease)
homologous chromosomes
the chromosomes from each parent that contain equivalent genes
homozygous
an organism has inherited the same alleles coding for a particular characteristic
heterozygous
- an organism has inherited different alleles coding for a particular characteristic
- the phenotype depends on which allele is dominant
genotype
the combination of alleles in genes
phenotype
the appearance/expression of the genotype
causes of genetic variation
- sexual reproduction
- genotype and phenotype
- dominant and recessive alleles
- homozygous and heterozygous genotypes
continuous variation
- a characteristic that can take any numerical value within a range
- caused by genetic and environmental variation
- polygenetic (controlled by a number of genes)
- graduation in values from one extreme to the other (continuum)
- usually plotted as a histogram
- e.g. height, mass, leaf surface area, skin colour
Discontinuous variation
- a characteristic that can only appear in specific (discrete) values
- mostly genetic
- controlled by one (monogenetic) or two genes
- normally presented in a bar graph or pie chart
- e.g. biological sex, bacteria shape, human blood groups
codominance
- when two different alleles that code for a gene are both equally dominant
- as a result both alleles of the gene are expressed in the phenotype of the organism if present
- e.g. if alleles for red and white flowers are both present (the plant is heterozygous) pink flowers are produced
Sex linkage
- some characteristics are determined by genes carried on sex chromosomes (sex linked genes)
- as the Y chromosome is a lot smaller than the X chromosome, there are a number of genes in the X chromosome that males only have one copy of
- this means that any characteristic caused by a recessive allele on the section of the X chromosome that is missing in the Y chromosome occurs more frequently in males
- e.g. haemophilia, colour blindness
- this is because many females will also have a dominant allele on their other X chromosome
haemophilia
- a sex linked genetic disorder
- the absence of a blood-clotting factor means injury can result in prolonged bleeding
- if a male inherits the recessive allele that codes for haemophilia on their X chromosome, they cannot have a corresponding dominant allele on their Y chromosome, so develop the condition
- the vast majority of haemophilia sufferers are male
- females who are heterozygous for the haemophilia coding gene are known as carriers as they do not suffer from haemophilia, but may pass the recessive allele on to their offspring
dihybrid cross
used to show the inheritance of two different characteristics caused by two genes, which may be located on different pairs of homologous chromosomes. Each of these genes can have two or more alleles
expected dihybrid inheritance ratio
9:3:3:1
why can the actual ratios observed in dihybrid crosses differ from those expected
- the fertilisation of gametes is a random process, so in a small sample a few chance events can lead to a skewed ratio
- the genes being studeied are on the same chromosome (autosomal linkage). If no crossing over occurs, the alleles for the two characteristics will be inherited together
autosomal linkage
the two genes that are linked are on the same non-sex chromosome (autosome)
- the closer the gene loci are to each other, the more likely they are to be inherited together as it is less likely crossing over will have an effect
- linked genes cannot undergo the normal random shuffling of alleles during meiosis, so the expected dihybrid ratios will not be produced in the offspring as the linked genes are effectively inherited as a single unit
recombinant offspring (autosomal linkage)
- have different combinations of alleles that either parent
- this is due to crossing over
- the closer the genes are on a chromosome, the fewer recombinant offspring produced
recombination frequency
- a measure of the amount of crossing over that has happened in meiosis
- number of recombinant offspring / total number of offspring
- 50% = there is no linkage, the genes are on separate chromosomes
- <50% = there is gene linkage, the random process of independent assortment has been hindered
- a recombinant frequency of 1% relates to a distance of one map unit apart on a chromosome