Topic 4B - Diversity, classification and variation ARN * Flashcards
meiosis and genetic variation mutations genetic diversity and natural selection investigating selection classification of organisms DNA technology, classification and diversity investigating variation biodiversity
what are gametes?
sperm cells in males and egg cells in females.
they join together at fertilisation to form a zygote, which divides and develops into a new organism
what is the diploid number?
the number of chromosomes normal body cells have, denoted 2n. so each cell contains 2 of each chromosome, 1 from each parent
what is the haploid number?
(n) half the number of chromosomes that normal body cells have. gametes have a haploid number of chromosomes - 1 copy of each chromosome
why do gametes have a haploid number of chromosomes?
so when they combine they form a cell with the normal diploid number. half from each gamete
what does random fertilisation produce?
zygotes with different combinations of chromosomes to both parents. this mixing of genetic material in sexual reproduction increases genetic diversity within a species
what is meiosis?
a type of cell division that takes place in the reproductive organs. cells that divide by meiosis start as diploid and form haploid cells
what happens to DNA before meiosis starts?
DNA unravels and replicates so there are 2 copies of each chromosome, called chromatids
the DNA condenses to form double-armed chromosomes, each made from 2 sister chromatids joined in their centres by a centromere
what happens in meiosis I?
chromosomes arrange themselves into homologous pairs
these pairs are then separated, halving the chromosome number
2 haploid cells produced
what happens in meiosis II?
the pairs of sister chromatids that make up each chromosome are separated (centromere divided)
4 genetically different haploid cells (gametes) are produced
how many chromosomes do humans have?
46 chromosomes, 23 homologous pairs
what are homologous pairs of chromosomes?
chromosomes that are the same size and have the same genes (alleles).
1 chromosome in each pair came from mum and 1 from dad
what is meiosis needed for?
sexual reproduction, as it produces daughter cells with half the number of chromosomes of the parent cell
when is the chromosome number halved during meiosis?
chromosome number halved during the 1st division.
as sister chromatids are pulled apart in 2nd but each chromatid is still counted as a chromosome
what is chiasmata form?
during meiosis I, homologous pairs of chromosomes come together and pair up. the chromatids twist around each other and some alleles swap over.
the chromatids still have the same genes, just different combinations of alleles
what does the crossing over of chromatids mean?
each of the 4 daughter cells formed from meiosis contains chromatids with different alleles
what is independent segregation of chromosomes?
its completely random which chromosome from each pair ends up in which daughter cell when homologous pairs are separated.
so the 4 daughter cells produced by meiosis have completely different combinations of those maternal and paternal chromosomes
how are the outcomes of mitosis and meiosis different?
mitosis - produces cells with same number of chromosomes as parent
meiosis - half the number of chromosomes
mitosis - daughter cells are genetically identical
meiosis - daughter cells are genetically different
mitosis - 2 daughter cells produced
meiosis - produces 4 daughter cells
how are the processes of mitosis and meiosis different?
mitosis - only 1 division
meiosis - 2 divisions
mitosis - no pairing or separating of homologous chromosomes, so no crossing over or independent segregation of chromosomes
meiosis - does
what is chromosome mutation?
when the daughter cells produced in meiosis don’t have the correct number of chromosomes due to errors during meiosis
what do chromosome mutations lead to?
inherited conditions, because the errors are present in the gametes (hereditary cells)
what is non-disjunction?
a failure of the chromosomes to separate properly.
what can non-disjunction of chromosome 21 do?
in humans, non-disjunction of chromosome 21 during meiosis an lead to Down’s syndrome
what is Down’s syndrome caused by?
a person having an extra copy of chromosome 21.
this happens when that chromosome fails to separate properly during meiosis, so 1 cell gets an extra copy of 21 and another gets none
when this cell fuses with another gamete at fertilisation, the resulting zygote will have 3 copies of chromosome 21
what are the types of mutations of the DNA base sequence?
substitution deletion insertion duplication addition translocation