Genetics, Biodiveristy And Classification Flashcards
How is DNA stored in Eukaryotic cells?
- Linear DNA that exist as chromosomes, each made up of one long molecule, found in the nucleus
- DNA is wound around proteins called histones
- DNA and the histones are coiled up very tightly to make a compact chromosome
- Mitochondria and chloroplast in eukaryotic cells also have their own DNA, which is circular and shorter.
How is DNA stored in Prokaryotes?
- Also carried as chromosomes, but are circular and shorter
- condenses to fit in by super coiling
What is a gene?
A sequence of DNA bases that codes for either a polypeptide or a functional RNA.
What is a genome?
The complete set of genes in the cell
What is a proteome?
The complete set of proteins a cell is able to produce
What is a non-coding repeat?
Regions of multiple repeated DNA outside of genes
E.g. CCTTCCTTCCTTCCTT they do not code for amino acid alongside introns
What is an allele?
Different forms of a gene, where the order of bases in each allele is slightly different so they code for slightly different versions of the same polypeptide
What are homologous pairs?
Pairs of matching chromosomes, they both are the same size and have the same genes, although they can carry different alleles, alleles coding for the same characteristic will be found at the same fixed position (locus) on each chromosome.
What is mRNA?
Made during transcription = messenger RNA
Carries the genetic doe from the DNA to the ribosomes, where it is used to make a protein during translation
- mRNA is a single polynucleotide strand, groups of three adjacent bases a called codons
What is tRNA?
tRNA is involved in translation
It carries the amino acids that are used to make proteins to the ribosomes
- tRNA is a single polynucleotide strand that is folded into a clover shape held to tether by hydrogen bonds
- every tRNA molecule has a specific sequence of three bases at one end called an anticodon
- they have an amino acids binding site
What happens during transcription?
1) DNA helicase breaks the hydrogen bonds between the two strands, exposing them to bases
2) RNA polymerase joins free nucleotides to the exposed bases, complementary base pairings means that the mRNA strand ends up being a complementary copy of the DNA template;ate strand, except the base T is replaced with U
3) hydrogen bonds reform and the strands coil back into a double helix
4) when RNA polymerase reaches a stop code it detaches from the DNA
5) mRNA three modes out of the nucleus through a nuclear pore and attaches to a ribosome in the cytoplasm
What happens during splicing?
Introns are removed leaving the exons joined together
Prokaryotic mRNA doesn’t have introns so no splicing necessary
What is the process of translation?
1) mRNA attaches itself to a ribosome and tRNA molecules carry amino acids to it, ATP provides the energy for the bond between the amino acids and the tRNA to form
2) tRNA with an anticodon that’s complimentary to the first codon on the mRNA attaches itself to the mRNA
3) a second tRNA molecule attaches itself to the next codon
4) the two amino acids are joined by a peptide bond
5) this continues all along the mRNA until a stop codon is reached
Why is the genetic code non-overlapping?
Each base triplet is read in sequence, superstate from the triplet before it and after it, bases don’t share their bases
How is the genetic code degenerate?
There are more possible combinations of triplets than there are amino acids, means that some amino acids are coded for by more than one base triplets
How is the genetic code universal?
The same specific base triplets code for the same amino acids in all living things
What are gametes?
Sperm and eggs cells (haploid) that fuse together in fertilisation to form a zygote (diploid) which develops into a new organism
What does haploid and diploid mean?
Haploid = only one copy of each chromosome
Diploid = each cell contains two of each chromosome, one from the mum and one from the dad
How can fertilisation cause genetic variation?
Fertilisation is random as it produces zygotes with different combinations of chromosomes to both parents, the mixing of the genetic material increases the genetic diversity within a species
What is the general process of meiosis?
1) before meiosis starts the DNA unravels and replicate = two copies of each chromosome called chromatids
2) DNA condense to got double-armed chromosomes made form two sister chromatids joined by a centromere
3) meiosis 1 the chromosomes arrange themselves int. homologous pairs which are then separated halving the chromosome number
4) meiosis 2 the pair of sister chromatids that make up each chromosome are separated, the centromere is divided
5) 4 haploid cells are made genetically different from each other
How does crossing over create genetic variation in meiosis?
During meiosis 1:
- homologous pairs of chromosomes pair up
- the chromatids twist around each other and bits of the chromatids swap over
- chromatids still contain the same genes but now have a different combination of alleles
How is genetic variation caused by independent assortment in meiosis?
When homologous pairs are separated in meiosis 1 it is completely random which chromosome from each pair ends up in which daughter cell
Compare the outcomes of meiosis vs mitosis?
Mitosis = cells with the same number of chromosomes as the parent cell, daughter cells are genetically identical, two cells
Meiosis = cells with half the number of chromosomes, genetically different, four cells produced
What is non-disjunction?
When chromosomes fail to separate properly
Can happen in meiosis 1 or 2
E.g. non-disjunction of chromosomes pair 21 can lead to Down Syndrome