Unit 2 exam Flashcards
what are genes
sequences of bases located on chromosomes that code for specific proteins (ATCG)
what do proteins from genes control
traits or characteristics of the organism
what are alleles
different forms of a particular gene
what is an example of a gene and a kind of allele
a gene would be eye colour and an allele of that gene is to have blue eyes
what is a genome
the complete set of genetic instructions for an organism (the total DNA)
how is a genome expressed
as the base sequence of the haploid set of chromosomes
how many chromosomes in a human
46, 23 pairs
how many autosomes in a human
44, 22 pairs
how many sex chromosomes in a human
2
Where do your 46 chromosomes come from
23 from father, 23 from mother
What are homologous chromosomes
matching pairs of chromosomes that have the same genes in the same places (same size)
what is the loci
the position of the gene on a chromosome
what is non-homologous
non-matching chromosomes
what are the 2 types of chromosomes
sex chromosomes and autosomes
how can autosomes be distinguished
the size, position of centromere and patterns of light and dark bands when stained
what is a karyotype
an image of chromosomes from a cell arranged in an organised manner
What do karyotypes do
allow us to see all the chromosomes and see if there is a wrong amount (diseases)
What are the 3 chromosome abnormalities
changes in the number of chromosomes, changes in a part of a chromosome, changed arrangements of chromosomes
what is trisomy
when an organism has an extra in a pair of chromosomes
what it monosomy
when an organism has one chromosome in a pair
what is a genotype
the combination of the particular alleles of a gene or genes that are present and active in a cell or in an organism
what is a homozygous genotype
when a particular gene comprises of two identical alleles, eg AA or aa
what is a heterozygous genotype
when a particular gene comprises of two different alleles, eg Aa
what is a phenotype
A phenotype is the observable or measurable characteristics of an organism. It is a product of the genotype and the environment.
what does codominance mean
when a heterozygote expresses both the dominant and the recessive trait of a gene in its phenotype
what does codominance normally entail
showing both phenotypes or both colours (not mixed)
what is incomplete dominance
appearance in a heterozygote of a trait that is between either of the trait’s homozygous phenotypes
what does incomplete dominance entail
merging of phenotypes or colours together
what are the factors of an autosomal dominant trait (3)
both sexes are featured, all affected people have at least one affected parent, cant reappear after having 2 non affected people
what are the factors of autosomal recessive traits (3)
trait can skip generations, parents that are not affected can have affected kids, if both parents are affected then all children will be as well,
what are some features of X-linked dominant traits (3)
a male with the trait only passes it to all daughters, it disappears if no one is affected, in large pedigrees more females are affected
what are some features of x-linked recessive traits (3)
affected mothers have affected sons, daughters of affected fathers are carriers, across a large pedigree more males will be affected
what is meiosis
sexual reproduction which halves the chromosome number to produce gametes
what are the stages of meiosis
PMAT i PMAT ii
what happens in interphase of meiosis
the DNA is replicated forming 4 chromosomes
what happens in prophase i
the chromosomes condense and nuclear envelope degrades, starting crossing over