INHERITANCE AND VARIATION Flashcards
Describe chlorosis
chlorosis is when the cells are not producing the normal amount of chlorophyll, reducing photosynthesis. Most plants with chlorosis have the normal genes coding for chlorophyll production. The change in their phenotype is a result of their environment.
What are the environmental factors causing chlorosis?
-lack of light: plants will turn off their chlorophyll production to conserve resources.
-mineral deficiencies (e.g lack of iron or magnesium): iron is needed as a cofactor by some enzymes that make chlorophyll and magnesium is found in chlorophyll molecule
-virus infections: viruses can interfere with metabolism of cells at the point they can no longer support the synthesis of chlorophyll.
Genetic variation is due to?
sexual reproduction involving meiosis (the formation of gametes) and the random fusion of gametes at fertilisation.
what is a genotype?
the genetic constitution of that organism (the alleles it has for a gene)
What is a phenotype?
the expression of the genes and its interaction with the environment
What is a dominant allele?
version of the gene that will always be expressed if present in an organism
What is a recessive allele?
version of gene that will only be expressed if two copies of this allele are present in an organism
what is homozygous?
a pair of homologous chromosomes carrying the same alleles for a single gene
what is heterozygous?
a pair of homologous chromosomes carrying two different alleles for a single gene
Describe continuous variation?
-a characteristic that can take any value within a range
-genetic and environmental causes
-polygenes (controlled by multiple genes)
-e.g animal mass, skin colour
Describe discontinuous variation?
-a characteristic that can only appear in specific (discrete) values
-mostly genetic causes
-one or two genes involved
-e.g blood group, albinism
How do you perform a genetic cross?
-state phenotype for both parents
-state genotype for both parents
-state gametes for each parent
-punnett square
-state proportion of each genotype which are produced in the offspring (ratio)
-state the corresponding phenotype for each possible genotype
what is codominance?
occurs when two equally dominant alleles occur for a gene. As a result both alleles for a gene are expressed in the phenotype of the organism if present.
Describe how blood group is determined by a gene with multiple alleles?
the immunoglobulin gene codes for the production of antigens on the surface of red blood cells. There are three alleles for this gene.
What is the male and female chromosome pair?
male- X Y
female- X X
Describe the X and Y chromosomes?
X chromosome is large and contains many genes not involved in sexual development. Y chromosome is very small, containing almost no genetic variation but it does carry the gene that causes the embryo to develop as a male
What is a sex-linked gene?
characteristics determined by genes carried on the sex chromosomes. As X chromosomes are much bigger than Y chromosomes, any characteristic caused by a recessive allele on the section of the X chromosome, which is missing on the Y chromosome, occurs more frequently in males
what is haemophilia?
sex-linked disorder in which blood clots extremely slowly due to the absence of a protein blood-clotting factor. This can lead to prolonged bleeding and if untreated can be fatal
How is haemophilia sex-linked?
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 and so develop the condition. Most haemophilia sufferers are male
What is a dihybrid cross?
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.
what is the expected ratio in a dihybrid cross between two heterozygous individuals?
9:3:3:1
why might the ratio not meet the expected ratio of 9:3:3:1?
-random fertilisation of gametes
-crossing over may have occurred disrupting the linked genes (genes on the same chromosome)
what is an autosome?
chromosome not concerned with sex determination
what is linkage?
genes are located on the same chromosome. Linked genes are inherited as one unit- there is no independent assortment during meiosis unless the alleles are separated by chiasmata.
What is autosomal linkage?
when the genes that are linked are found on one of the other pairs of chromosome
what are recombinant offspring?
have a different combination of alleles than either parent. The closer the genes are on a chromosome, the less likely they are to be separated during crossing over and fewer recombinant offspring produced.
what is recombination frequency?
a measure of the amount of crossing over that has happened in meiosis.
recombination frequency equation?
number of recombinant offspring/ total number of offspring
A recombination frequency of 50 percent indicates?
indicates that there is no linkage and the genes are on separate chromosomes.
A recombination frequency of less than 50 percent indicates?
indicates that there is gene linkage and the random process of independent assortment has been hindered.