topic 4 Flashcards
differences between DNA and RNA
DNA: -double stranded -contains the base thymine -contains deoxyribose sugar -much longer than RNA -found in the nucleus RNA: -single stranded -contains the base uracil -contains ribose sugar -shorter than DNA -found in the cytoplasm
what are nucleotides and what do they consist of
nucleotides are the monomers that make up DNA and RNA. they join together in condensation reactions by phosphodiester bonds.
they consist of pentose, a nitrogenous base and a phosphate group.
features of the genetic code
genetic code - order of bases on DNA
- universal so all known living organisms use the same genetic code.
- non overlapping so each triplet is only read once and triplets don’t share any bases
- genes are separated by non-coding multiple repeats of base sequences
- degenerate so more than one triplet codes for one amino acid
- contains stop and start codons
what are non-coding and coding sections of DNA called
non-coding - introns
coding - exons
what is a gene
the sequence of bases on a DNA molecule coding for a sequence of amino acids in a polypeptide chain. it occupies a fixed position called a locus on a particular DNA molecule
DNA in eukaryotic cells vs prokaryotic cells
eukaryotic cells:
-the DNA molecules are found in the nucleus and are long and linear.
-they wind around proteins called histones to fit in the nucleus.
-the DNA and histone coil very tightly to form chromosomes.
-the mitochondria and chloroplasts contain short circular DNA.
prokaryotic cells:
-the DNA is short and circular and not associated with proteins.
-condenses to fit in the cell by supercoiling
what is the genome
the complete set of genes in the cell
what is the proteome
the full range of proteins that the cell is able to produce
allele
a different form of a gene
describe a homologous pair of chromosomes
both chromosomes are the same size and have the same genes but could have different alleles
describe mRNA
- made during transcription
- carries the genetic code from the DNA to the ribosomes where it is used to make proteins during translation
- it is a single-stranded linear molecule
- groups of 3 adjacent bases are called codons
describe tRNA
- involved in translation
- carries amino acids that are used to make proteins to the ribosomes
- it is a single-stranded molecule folded into a cloverleaf shape.
- held together by H bonds between specific base pairs
- anticodon at one end of the molecule and an amino acid binding site on the other end.
describe the process of transcription
transcription is the process where a DNA strand acts as a template to form a complementary mRNA strand
in prokaryotes, this occurs in the cytoplasm
in eukaryotes, this occurs in the nucleus
-an enzyme called DNA helicase breaks the H bonds between the two strands in a DNA double helix causing the DNA to unwind, exposing its bases.
-one strand known as the antisense is used as a template to make an mRNA copy.
-free floating nucleotides line up according to complementary base pairing with the DNA template strand except uracil replaces thymine.
-this forms mRNA
-the enzyme RNA polymerase catalyses the formation of phosphodiester bonds between each base in the mRNA strand, forming an mRNA molecule
-when the RNA polymerase reaches a stop codon, the mRNA stops being made
mRNA produced is eukaryotes vs prokaryotes
- in eukaryotes, the introns and exons are both copied into mRNA during transcription.
- mRNA containing introns and exons is called pre-mRNA.
- the pre-mRNA is spliced by spliceosomes to remove introns.
- the mRNA then moves out of the nucleus through nuclear pores and attaches to a ribosome in the cytoplasm.
- in prokaryotes, mRNA is produced directly from the DNA.
- splicing doesn’t take place because the mRNA doesn’t contain introns.
what are gametes
sex cells
sperm and egg cell
what is a zygote
a fertilised egg in early stages of development
diploid
normal body cells have the diploid number of chromosomes so each cell contains two of each chromosome.
haploid
gametes have a haploid number of chromosomes - there’s only one copy of each chromosome.
describe the process of translation
when the polypeptide chain is produced
- once the modified mRNA has left the nucleus, it attaches to a ribosome in the cytoplasm
- the ribosome attaches at the start codon
- free tRNA molecules bind with their specific amino acids in the cytoplasm and bring them to the mRNA molecule on the ribosome
- The triplet of bases (anticodon) on each tRNA molecule pairs with a complementary triplet (codon) on the mRNA molecule
- Two tRNA molecules fit onto the ribosome at any one time, bringing the amino acid they are each carrying side by side
- A peptide bond is then formed between the two amino acids
- The formation of a peptide bond between amino acids requires energy, in the form of ATP
- The ATP needed for translation is provided by the mitochondria within the cell
- This process continues until a ‘stop’ codon on the mRNA molecule is reached – this acts as a signal for translation to stop and at this point the amino acid chain coded for by the mRNA molecule is complete
- This amino acid chain then forms the final polypeptide
what is rRNA
ribosomal RNA makes up the bulk of ribosomes
what is the purpose of meiosis
-consists of two nuclear divisions which results in the formation of four haploid daughter cells from a single diploid parent cell that are genetically different
how does meiosis introduce variation
-independent segregation
-crossing over
both occur in the first round of division
how many chromosomes are in each division
46–>92—> two cells, each with 46–> 4 cells each with 23
describe crossing over
during meiosis 1, homologous pairs of chromosomes come together and pair up. the chromatids on each chromosome twist around each other and sections of the chromatids swap over. the chromatids still have the same genes but now have a different combination of alleles. this increases genetic variation.
describe independent segregation of chromosomes
- when the homologous pairs are separated in meiosis 1, it is completely random which chromosome from each pair ends up in which daughter cell
- this means that the 4 daughter cells have completely different combinations of the maternal and paternal chromosomes.
- this leads to genetic variation.
how does random fertilisation increase genetic variation
during sexual reproduction, fertlisation is random so any sperm cell can fertilise any egg cell. this produces zygotes with different combinations of chromosomes to both parents and increases genetic variation.
what are the different outcomes from meiosis and mitosis
- mitosis produces cells with the same number of chromosomes as the parent cell whereas meiosis produces daughter cells with half the number of chromosomes as the parent cell.
- in mitosis, the daughter cells are genetically identical to each other and the parent cell. in meiosis, each daughter cell is genetically different from each other and the parent cell.
- mitosis produces two daughter cells whereas meiosis produces four daughter cells.