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Author Topic: quick recap I MEAN REALLY QUICK  (Read 900 times)  Share 

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bar0029

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quick recap I MEAN REALLY QUICK
« on: October 28, 2010, 09:57:29 pm »
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genome: total sum of genetical material in a cell or the organism

gene expression: the process of protein synthesis which includes transcription, modification in euk., translation and modification at the golgi.

genes are the units of inheritence which are passed on to each generation

transcription: rna polymerase binds to the promotor sequence of the gene under consideration causing it to unwind exposing free nucleotides on the template strand. rna nucleotides are added to the exposed nucleotides according to the complementary base pairing rule with the aid of rna polym. this continues until the terminator is reached and mRNA is produced in prokaryotes and pre-mRNA in eukaryotes

translation: mRNA binds to the ribosome and the codons are read. tRNA attaches to a specific amino acid in the cytosol of which it carries to the ribosome. if the anti-codon is complimentary to the codon according to the complimentary base pairing rule, then the amino acid forms a part of the amino acid sequence. this process continues and adjacent amino acids are joined by peptide bonds. this stops when the stop codon is reached and the result is a polypeptide or protein.

gel electrophoresis: because dna is negatively charged, the negative electrode results in the dna being repelled by the negative electrode. the longer the length of the DNA, the greater the frictional resistance for the DNA to pass through the agarose gel.

DNA profiling: basically looks at using short tandem repeats, which is run through gel electrophoresis and can be compared.

DNA sequencing: helps determine the base nucleotide sequence of a DNA strand. it is based on the fact that each nucleotide stains differently, and so can be readily identified in a strand.

DNA recombination: this involves cutting a plasmid and a transgene with the same restriction enzyme. in doing so, the plasmid and transgene can hybridise due to complimentary base pairs. the gene is then incorporated into the genome of the prokaryote and thus the gene will be expressed, producing the desired product e.g. human insulin.

DNA amplification: involves amplifying the amount of DNA when a trace amount is present. first of all the dna sample is heated in order to denature the DNA ensuring that the strands are single stranded. it is then cooled and primers are added at the 3' end. it is then heated to anneal primers. dna nucleotides are then added according to the complimentary base pairing rule with the aid of dna polymerase. this cycle continues.

gene cloning: the process of producing genetically identical cells or offspring to the donor. there is therapeutic which involves the production of tissues etc. and there is reproductive which is the production of an entire organism. the methods are nuclear transfer and embryo splitting.

gene transformation: mannipulate a gene so that the functioning of the gene has also been altered. this is basically the same thing as recombination.

gene delivery systems: these vectors that are used depend on the organisms which are involved, can use retroviruses, adenoviruses, microinjection, agrobacterium, liposome etc.

gene regulation: in prokaryotes they have operons, and they produce repressor molecules from regulatory genes which inhibit the expression of a gene. in eukaryotes we have dna binding proteins and signalling proteins. it conserves energy so that energy is not wasted on maintaining genes which are not required and also allows the differentiation of cells.

eukaryote chromosomes are made up of 1/3 dna and 2/3 protein.

alleles are alternative forms of a gene

[prokaryote chromosomes are found as a circular molecule alongside numerous plasmids which are self-replicating double stranded circular molecules of dna., note the circular molecules is found on the circular chromosome.

cell cycle: a representation of the different phases that a cell goes through, throughout its lifetime. gap 1, synthesis, gap 2 and replication. in gap 1: cell is growing, organelles doubling, in synthesis dna replication occurs, in gap 2 cell is preparing for mitosis./ binarry fission/ meiosis.

DNA replication: process is known, but important enzymes need to remmeber are dna helicase, dna primase, dna polymerase, dna ligase

apoptosis: programmed cell death.. deaths signals are picked up by death receptors activating self-destruction. capsases are activated and break down protein and dna, phagocytosis of parts of the cell occurs and other parts e.g. organelles are recycled.

binary fission: the form of cellular replication in prokaryotes whereby one cell gives rise to two genetically identical daughter cells with the same genome.

meiosis: inputs: diploid cell.. outputs: 4 genetically diverse haploid cells

mutations: random permeanent changes in the dna of an individual which can alter the seuqence or the arrangement of. the mutation can be a point mutation or a macro/ black mutation. it is the source of new alleles in a population.,

genotype: the specific alleles that an individual posses at a particular gene locus.

phenotype: the way that the genotype os expressed biochemically, structurally, behaviourally or physiologically which is a product of both the genotype and the environment.

continous: when a trait varies over a continuum and no discrete groups can be distinguished e.g. eye colour

discontinuous: when thre are only specific variations of a trait e.g. ABO blood groups.





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bar0029

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Re: quick recap I MEAN REALLY QUICK
« Reply #1 on: October 28, 2010, 10:08:02 pm »
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still more to come...

gene pool: the total sum of alleles present in a population.

allele frequency: the prevalence of an allele in a population which is on a scale from 0-1

selection pressures: forces of natural selection which can select for or against a particular trait under certain environmental conditions.

genetic drift:  random change in the allele frequency of a population in only a couple of generations which has a greater affect on smaller populations. there is bottleneck which affects the original population forming a genetically simplified population. there is founder which is when a group of members from a population go on to inhabit a new area which is isolated where no gene flow exists with the previous, whereby the new founder population is not a representative of the original population.

natural selection:
1. there was variation
2. change in environment so there was a struggle for survival
3. the fittest were able to survive in the new environment
4. change in allele frequency and those that were fittest were able to survive to reproductive age so that the prevalance of the allele responsible for the favourable allele is high

relative dating: a form of dating which results in qualitative ages of fossils, e.g. stratiphication which based on the principle of correlation

actual/ absolute dating technique: a quantitative date is given which is determined with the use of radioisotopes e.g. carbon 14 and also electron spin resonance. \

evidence for evolution:
biochemical, anatomical structures, distribution, fossilisation, embryos, witnessing

divergent: when one or more species arise from a common ancestor who are more evolved and show structures that were present in the ancestor but may have different funcions

convergent: when one or more species develop structures which have similar functions but have evolved independently as they have been exposed to similar selective pressures.

allopatric speciation; speciation which has resulted due to a small population being geographically isolated from the original, hence new adaptations in different environments.

extinction: total loss of an allele or speicies from the earths biodiversity.


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onerealsmartass

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Re: quick recap I MEAN REALLY QUICK
« Reply #2 on: October 28, 2010, 10:10:27 pm »
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wow good job :D

shinny

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Re: quick recap I MEAN REALLY QUICK
« Reply #3 on: October 28, 2010, 10:10:58 pm »
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I've uploaded these several times before but here they are once again. And yeh, they're not my notes. Author's stated somewhere inside the document. Enjoy!
MBBS (hons) - Monash University

YR11 '07: Biology 49
YR12 '08: Chemistry 47; Spesh 41; Methods 49; Business Management 50; English 43

ENTER: 99.70