Study of genes and their transmission from one generation to the next
Genes
DNA sequences that contain instructions for building proteins
Genome
Sum total of all of the organism's DNA
Meiosis
Genetically different from the parents and the 4 daughter cell is different from itself on prophase when crossing over happens and on anaphase 1 where the homologous chromosomes separate
Genes
DNA
DNA
Chromosomes
Chromosomes
Genome
Genotype
All the sets of alleles, complete set of alleles
Phenotype
Characteristics that are expressed, physical and biochemical structure such as blood or observable functional traits
Chromosomes
Structures within the nucleus, composed of DNA & protein
Humans have 46 chromosomes and 23 pairs
First 22 are AUTOSOMES & last 1 pair is an ALLOSOME (sex chromosomes where XX is female and XY for male)
Karyotype
Procedure where we identify and evaluate the size and shape of the chromosomes to see if there are missing or extra chromosomes (mutations)
Karyotype is arranged from largest to smallest chromosomes
Karyotype doesn't include the last chromosomes
Karyotyping
Important to find out if you have mutation in sex cell to know if you will pass it down
Karyotyping
You can identify if it is a homologous pair by its size, shape, and centromere location
Each chromosome carries a specific gene
Karyotype
A composite visual display of all of the chromosomes of an individual
Karyotype
Shows all 23 pairs of chromosomes lined up side-by-side
Karyotype
We evaluate the Size, Shape, and Number of Chromosomes
Karyotype
Chromosomes are arranged from the largest to the smallest
Karyotyping
You'll find out the alterations or mutations, especially if it is in your sex cells, will have a chance of it being passed down to your baby
Stillborn—baby born dead
Karyotyping
Aside from the size, you can look at the location of their centromeres to find out if the two are homologous
Autosomes
Parts can also be found in allosomes
Pair of autosomes
Each autosome carries the same genes at the locus
Gene locus
The location of a specific pair of genes
Pair of genes
Normally, both genes have the same structure and function
Alleles
Alternative versions of the same gene pair
Color blindness is more common in males
Dominant allele
Always expressed whether homo or hetero, expressed with a capital letter, masks or suppresses the expression of its complimentary allele
Recessive allele
Only expressed if homozygous, expressed by small letter, will not be expressed if paired with a dominant allele (heterozygous)
Dominant alleles are not always more common than recessive ones; sometimes they may be rare in a population
Homologous chromosomes
One member of each pair is inherited from each parent, look alike (size, shape, banding pattern), not identical: may have different alleles of particular gene
Homozygous
The homologous pair are carrying identical alleles at the same location
Heterozygous
Two different alleles at a specific location
Hemizygous
Found only in X or Y; Only one allele
Color Blindness allele is hemizygous
Gregor Johann Mendel
Father of Genetics, experimented and worked on the garden pea plants (by breeding them) in the 1850's in Austria