Inheritance Flashcards
Meiosis vs mitosis
- meiosis leads to non-identical cells
being formed - mitosis leads to identical cells being formed
Sexual vs asexual reproduction
sexual
- involves the joining (fusion) of male and female gametes:
* sperm and egg cells in animals
* pollen and egg cells in flowering plants
- mixing of genetic information=variety in the offspring
- formation of gametes involves meiosis
Asexual
- only one parent and no fusion of gametes
- no mixing of genetic information
- genetically identical offspring (clones)
- Only mitosis is involved
cell division: meiosis
a cell divides to form gametes
- it copies its genetic information (chromosomes make identical copies of themselves)
- similar chromosomes pair up
- sections of DNA get swapped=cross-over=variation
- pairs of chromosomes divide
- cell divides in 2 and then the 2 cells divide again=4 gametes each with a single set of chromosomes
- all gametes are genetically different from each other
when do gametes join?
- gametes join at fertilisation to restore the normal number of chromosomes
- new cell divides by mitosis=number of cells increases
- as the embryo develops cells differentiate
pros and cons of sexual reproduction
pros
* produces variation in the offspring=if the environment changes variation gives a survival advantage by natural
selection which can be speeded up by humans in selective breeding to
increase food production
cons
- takes time and energy to find mates
- difficult for isolated members of the species to reproduce
pros and cons of asexual reproduction
pros
- only one parent needed
- more time and energy efficient as do not need to find a mate
- faster than sexual reproduction
- many identical offspring can be produced when conditions are favourable
cons
- limited genetic variation in population (all offspring is genetically identical to their parent)
- population is vulnerable to changes in the conditions and may be only suited for one habitat
- disease is likely to affect the whole population as there’s no genetic variation
how do organisms reproduce?
- Malarial parasites reproduce asexually in the human host, but sexually in the mosquito
- Many fungi reproduce asexually by spores but also reproduce sexually to
give variation. - Many plants produce seeds sexually, but also reproduce asexually by runners such as strawberry plants, or bulb division such as daffodils
what is DNA and where is it found?
- a polymer made up of 2 strands to form a double helix shape
- in the nucleus’ genetic material, contained in chromosomes
what is a gene?
a small section of DNA on a chromosome
what does a gene code for?
a particular sequence of amino acids, to make a specific protein
what is a genome?
the entire genetic material of that organism
why is the human genome project important?
- allows scientists to identify genes that are linked to different types of diseases=develop effective treatments
- trace migrations of certain populations of people around the world
- gives us an understanding of inherited disorders and can help develop treatments
what is DNA?
a polymer made of repeating nucleotide units different nucleotides
what is a nucleotide made of?
- a sugar and
phosphate group=backbone which alternate - one of four different bases attached to the sugar
what are the 4 bases and how do they pair up?
- A (adenine)
- C (cytosine)
- G (guanine)
- T (thymine)
- a+t & c+g pair together=complimentary base pairing
- joined by weak hydrogen bonds
what do 3 bases code for?
an amino acid
- order of bases control the order in which amino acids are assembled to form a protein
structure of DNA
double-helix
protein synthesis
transcription - copying of DNA
- DNA molecule is unzipped around the gene
- DNA is a double stranded molecule so it needs to be unzipped to expose one strand
- single strand of DNA acts as a template
- RNA polymerase helps make a copy of DNA as mRNA
- RNA polymerase binds to the non-coding region in front of a gene on one of the DNA strands and uses free nucleotides to produce a complementary mRNA strand of the coding part of the gene
Translation
- mRNA leaves the nucleus, moves into the cytoplasm and attaches to the ribosome
- tRNA molecules complementary to the mRNA arrive at the ribosome
- when the mRNA moves to the ribosome, it recruits tRNA that are complementary to the base sequence of the mRNA
- the tRNA has an anti-codon that is complementary to the mRNA’s codon
- the tRNA molecule carry amino acids with it
- the bases on the mRNA are read in threes and code for a specific amino acid
- the amino acids then bond with another and polypeptides are formed
- a polypeptide chain is formed and released and then folds in a specific shape to make a protein
why is the shape of a protein important?
the unique shape enables the proteins to do their job
types of protein
enzymes - biological catalysts
hormones - used to carry messages around the body
structural eg. collagen (strengthens connective tissues eg. ligaments or cartilage) - physically strong
How does the structure of DNA affect protein synthesis?
it determines the sequence of nucleotides, which determine the sequence of amino acids in proteins
- during protein synthesis, DNA is transcribed into RNA, which is then translated into proteins based on the sequence of nucleotides
- any changes in the DNA sequence can alter the resulting protein and potentially affect its function
how does variation of the coding parts of DNA affect the phenotype
- a strand of DNA is organised into sections of coding DNA (genes), separated by sections of the non-coding DNA
- if a mutation happens=DNA bases may be changed, added, or deleted=changes the sequence of bases, so the order of bases in mRNA produced during transcription may be different
- the amino acid may be assembled in a different order=wrong protein produced, or it may fold incorrectly and form a different shape eg. if the protein is an enzyme, it’s active site may change shape=no longer be able to bind to its substrate and catalyse a specific chemical reaction
how does variation in the non-coding parts [switch genes on and off=control if they’re expressed or not (used to make a protein)] of DNA affect the phenotype
- there are specific sequences of DNA bases found before a gene which trigger the process of transcription which are found in the non-coding sections of DNA
- if a mutation occurs in this sequence, the gene may not be transcribed into the mRNA=protein the gene codes for will not be produced
what is a mutation?
random change in an organism’s DNA and can be inherited
when do mutations occur?
continuously
- most do not alter the protein, or only alter it slightly so that its appearance or function is not changed
- few mutations code for an altered protein with a different
shape eg. enzyme may no longer fit the substrate binding site or a structural protein may lose its strength
- if there’s a mutation in the non-coding part of DNA, it alters how genes are expressed
types of mutations
- insertions - a new base is inserted into the DNA sequence where it shouldn’t be & has a knock-on effect on bases further down
- deletions - a random base is deleted from the DNA sequence & has a knock-on effect on bases further down
- substitutions - a random base in the DNA sequence is changed to a different base
what is a gamete?
a sex cell
what is a chromosome?
a molecule made up of many coiled up sections of DNA
what is an allele?
different forms of the same gene
what is a dominant allele?
more powerful allele
always expressed
represented by an uppercase
what is a recessive allele?
less powerful allele
only expressed if there’s two of them therefore no dominant allele
represented by a lowercase
what is a homozygous?
both of the same allele
can be either homozygous dominant or homozygous recessive