the joining and mix of male and female gametes to produce genetically different offspring by meiosis
What are gametes?
sex cells, haploid
how many chromosomes does a cell have
46
how many chromosomes does a gamete have
23
What is asexual reproduction?
The production of genetically identical haploid offspring from a single parent by mitosis.
advantages of sexual reproduction
genetic variation
allows selective breeding
disadvantages of sexual reproduction
slower process as organism has to find a mate
Advantages of asexual reproduction
-Only one parent needed
-More time and energy efficient as only need to find one mate
-Faster than sexual reproduction
-Many identical offspring can be produced when conditions are favourable
Disadvantages of asexual reproduction
no genetic variation
What is mitosis?
The division of one cell into two genetically identical diploid daughter cells in asexual reproduction
What is meiosis?
cell division that results in four genetically identical haploid daughter cells
process of meiosis
- The cell makes copies of its chromosomes so it has double the amount of genetic information
- Cell divides into two cells each with half the amount of chromosomes (46)
- The cell divides again producing four cells each with a quarter of the chromosomes (23)
DNA STRUCTURE
a polymer found in chromosomes in the nucleus. made up of two dna strands which are twisted together to form a double helix. made up of nucleotides with four different complementary bases
what is a gene
A section of DNA that codes for amino acids which are joined to make a protein
what are nucleotides made up of
sugar, phosphate, base, weak hydrogen bonds between bases
four organic bases
A,T
C,G
what is a genome
The entire set of genetic material in an organism
practical: extracting dna from fruit
- mix cold water, salt and washing up liquid
- pulverise the fruit to break down cell membrane
- add the solution and filter it with a sieve
- add ice cold ethanol so dna precipitates out
process of transcription
- RNA polymerase binds to non coding region in front of a gene and moves along.
- the two strands are pulled apart and complementary bases pair together to form a strand of mRNA
- the mRNA moves out of the nucleus through the nuclear pore and through the cytoplasm to be attached to a a ribosome
process of translation
- the mRNA leaves the nucleus through the nuclear pore, through the cytoplasm and binds onto a ribosome
- tRNA carries amino acids to ribosome
- tRNA bases match to complementary base pairs of mRNA in triplet code
- amino acids are joined to make a polypeptide which folds to produce a protein
what is a genotype
genetic makeup of an organism
What is a phenotype?
physical characteristics of an organism
what is a coding dna
sequence of DNA that codes for a protein that can alter sequence of amino acids
what is a non coding dna
regions of DNA that do not code for proteins, control gene expression
Who was Gregor Mendel?
Austrian monk who worked in monastery gardens and observed the characteristics passed onto the next generation of plants by carrying out breeding experiments on peas
mendels experiment conclusions
offspring have some characterises that their parents have - hereditary units
units can be dominant or recessive and cannot be mixed
Why is Mendel's work important?
mendel published his work in 1866 but was not recognised until after his death as genes were not yet discovered.
what are alleles
Different forms of a gene
Homozygous definition
when both alleles are the same
Heterozygous definition
when one of the alleles is dominant and the other recessive
What is a zygote?
diploid fertilized egg
family pedigree: unaffected female
white circle
family pedigree: black square
affected male
What does the 23rd pair of chromosomes determine?
gender
female genotype
XX
male genotype
XY
What is codominance?
when both alleles contribute to the phenotype: IA and IB
A and O alleles
IA
Why are sex-linked disorders more common in males than in females?
Males only have one X chromosome, so all X-linked genes are expressed in males, even if they are recessive. For females to get the gene, it would have to be linked to both X chromosomes.
how do mutations occur
when the sequence of bases are changed, potentially affecting the phenotype.