When plants are grown in dark there is a lot of phytochrome; almost all in form of Pr
When Pr is exposed to sunlight it is converted to Pfr
Has been shown that in presence of Pfr, seedlings grow normally, however in absence of Pfr, seedlings grow tall (etiolated)
Somehow the Pr triggers the plant to share available materials in favour of growing tall - stopping production of chlorophyll (chlorosis)
What is chlorosis?
when cells stop producing normal amounts of chlorophyll
this lack of chlorophyll can result in leaves looking pale/ yellow
Causes of chlorosis
lack of light - in absence of light plants will turn off chlorophyll production to conserve resources - chlorosis only occurs in dark
mineral deficiencies - e.g. lack of iron or magnesium that help produce chlorophyll
virus infections - interfere with plant metabolism & chlorophyll synthesis
How is animal body mass determined?
combo of genetic & environmental factors
environmental - determined by amount of food consumed, quantity of exercise, presence of disease
genetic - mutations can cause pattern of fat deposition in body to be altered
Genotype
genetic makeup of an organism
Phenotype
observable characteristics of an organism
Dominant allele
version of the gene that will always be expressed if present in an organism
Recessive allele
version of gene that will only be expressed if 2 copies are present in an organism
Homozygous gene
they have 2 identical alleles for a characteristic
can be homozygous dominant (contain 2 alleles for dominant phenotype) or homozygous recessive (contain 2 alleles for recessive phenotype)
Heterozygous gene
have 2 different alleles for a characteristic
the dominant allele will be expressed
Discontinuous variation
a characteristic that can only appear in specific values
qualitative
limited number of traits, no immediate forms
controlled by one or 2 genes usually with multiple alleles
mostly genetic causes - environment has little effect
presented on bar chart
Continuous variation
a characteristic that can take any value within any range
quantitative
range or gradation of characteristics
controlled by 2 or more genes (polygenic)
environment has significant effect
presented on line graph
Examples of discontinuous variation
Human blood groups
Albinism
Round & wrinkled pea shapes
Antibiotic resistance
Examples of continuous variation
stem height in plants
milk yield in cows
animal mass
skin colour
How does sexual reproduction lead to genetic variation within a species?
Crossing over
Reassortment of chromosomes
Reassortment of chromatids
Fertilisation
Mutation
Crossing over
at prophase I non-sister chromatids wrap around each other at points called chiasmata & these sections swap over
these sections contain same genes but diff alleles
Reassortment of chromosomes
metaphase I - maternal & paternal chromosomes align at random
each gamete acquires a diff mixture of maternal & paternal chromosomes
Reassortment of chromatids
metaphase II - sister chromatids align randomly
this determines how they segregate at anaphase II
results in sister chromatids no longer being genetically identical
Fertilisation
genetic material from 2 unrelated individuals is combined to make a zygote
2 main causes of genetic variation
mutation
sexual recombination
How does mutation cause genetic variation?
Deletion, addition or substitution of a nucleotide
Deletion or translocation of part of a chromosome
Aneuploidy - loss or gain of a single chromosome
Polyploidy - addition of whole chromosome sets
Why is variation essential in selection?
when environmental conditions change, genetic variety enables those individuals which are best adapted, to survive & reproduce, passing on their advantageous alleles to their offspring
Plus more of the offspring may have features that are MORE beneficial to the farmers who are growing/ rearing them
Monogenic inheritance
characteristic inherited on a single gene
Test Cross (not on spec but comes up in application Q so useful to know)
Determines whether an organism showing the dominant phenotype is homozygous or heterozygous
Involves crossing the organism w another that is homozygous recessive for the trait
If any of the offspring show the homozygous recessive trait in the phenotype, the parent must have been heterozygous
Steps in drawing a genetic cross
State phenotype of both parents
State genotype of both parents
State gametes of both parents
Draw punnett square
State proportion of each genotype
State corresponding phenotype
Codominance
when 2 diff alleles for a gene are equally dominant so are both expressed in the phenotype of a heterozygote
Example of codominance
an allele codes for red flowers
an allele codes for white flowers
3 colours can be produced
red flowers - plant is homozygous for allele coding for red
white flowers - plant is homozygous for allele coding for white
pink flowers - plant is heterozygous - single allele present which codes for red pigmentation produces enough pigment to produce pink flowers
How is blood group determined?
By a gene with multiple alleles
as an organism carries only 2 versions of the gene (one on each homologous chromosome) only 2 alleles can be present in an individual
Gene I codes for production of diff antigens on surface of RBC
I^A - results in production of antigen A
I^B - production of antigen B
I^O - production of neither antigen
I^A & I^B are codominant whereas I^O is recessive to both of the other alleles - diff combos of these alleles result in 4 blood groups
group A - IAIA or IAIO
group B - IBIB or IBIO
group AB - IAIB
group O - IOIO
Determining sex in mammals vs birds
in mammals females are homogametic (XX) & males are heterogametic (XY)
in birds, butterflies & moths, females are heterogametic (XY) & males are homogametic (XX)
Linkage
2 or more genes present on the same chromosome that are normally inherited together
Sex linkage
characteristics determined by genes carried on sex chromosomes - these genes are sex linked
as the Y chromosome is smaller than X chromosomes , there are a number of genes in the X chromosome that males only have one copy of
means any characteristic caused by a recessive allele on the section of the X chromosome (which is missing on Y) occurs more frequently in males - because many females will also have a dominant allele present in their cells
Example of a sex-linked genetic disorder
haemophilia
Haemophilia
patients have blood clots caused by a recessive allele that encodes non-functioning Factor VIII (protein blood-clotting factor)
gene for Factor VIII is located on the X chromosome - haemophilia is sex linked
if a male inherits recessive allele that codes for haemophilia they cannot have a corresponding dominant allele on Y chromosome & so develop condition
females who are heterozygous for gene are known as carriers
Dihybrid inheritance
inheritance of 2 genes
Dihybrid cross
shows inheritance of 2 diff characteristics caused by 2 genes, which may be located on diff pairs of homologous chromosomes
each of these genes can have 2 or more alleles
What can we work out from a dihybrid cross?
the diff phenotypes expected
the ratio of diff phenotypes and genotypes expected from the cross
Stages of dihybrid cross
F1 cross
gamete formation
F2 cross
F1 cross
2 homozygous parents w opposite alleles are bred together - one has dominantalleles, other has recessive alleles
all offspring in F1 generation will have a heterozygousgenotype (e.g. YyRr)
2 homozygous parents w opposite alleles are bred together - one has dominant alleles, other has recessive alleles
all offspring in F1 generation will have a heterozygous genotype (e.g. YyRr)
Gamete formation (dihybrid cross)
each F1 parent (e.g. RrYy) can produce 4 possible gametes due to independent assortment
RY, Ry, rY, ry
F2 cross
2 heterozygous parents are bred together (using offspring of F1)