Genetics Flashcards
DNA profiling and steps
Generating a pattern of bands from a DNA sample to be analysed
1. Release DNA
2. CUT DNA INTO FRAGMENTS USING ENZYMES
3. Separate on basis of size
4. Fragments create a pattern
What is a Gene
A section of DNA that codes for a particular protein
On chromosomes (locus)
Homologous Pairs: genes of similar trait
22 autosomes
23 sex chromosomes
heriditary and allele
The passing of features and traits from parent to offspring by means of genetics
Allelus are dominant or recessive
Heterozygous
Homozygous
Genotype/Phenotype
Phenotype: Brown Eyed - physical makeup
Genotype Bb - genetic makeup
Genetic Crosses
2 parents on sides of punnet square
Sex Linkage
The gene for a particular condition is located on a sex chromosome (X or Y)
XY - Male
XX - Women
Sperm controls sex of progeny (child)
Genes that control traits are found of the sex chromosomes (X)
Sex linked condition: Haemophilia
Law of Segregation
Traits are controlled by pairs of factors (alleles) which separate at gamete formation
Each cell contain two factors for each trait
Each gamete contains only one factor, fertilisation makes 2 factors
Mono hybrid crosses
Pea plants: purple and white
Alleles: ppairs of factors - heriterable traits
Law is Independent Assortment
Members of a pair of factors (alleles) separate independently from members of another pair at gamete formation
9:3:3:1: heterozygous with heterozygous
1:1:1:1: heterozygous with homozygous
(If genes are linked, law will not apply)
Eukaryotic chromosome structure
Many linear chromosomes
Supercoied DNA
2 copies of genome, condensed, centromere and arms, X shaped
Chromosomal Theory of Inheritance
Chromosomes occur in matched pairs
46 number of chromosomes: 23 pair of homologous replicated chromosomes, with centromere and sister chromatids
Meoisis = n=23
mutations: types and causes
Genones alter slowly over time, beneficial traits survive (natural selection)
Genetic Variation: difference in DNA/alleles
Mutuations:
Chromosomal (incorrect number, translocation)
Gene: change in the amount or structure of DNA - deletions, insertions, substitution
Cause: exposure to mutagens,radiation, spontaneously
Protein Synthesis
Code from gene in DNA in nucleus is copied from the gene (single stranded so can fit through nuclear pores
) to ribosomes (protein - making)
- Initiation: DNA unwinds by enzymes breaking the strands apart
- Transcription: making mRNA using DNA as a template (complementary bases align) messenger rna then leaves nucleus and go to ribosomes
- Translation: tRNA in the cytoplasm carry the correct amino acid to connect through peptide bonds and chain continues to stop codon
- Protein folding