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Unit 8 - Coggle Diagram
Unit 8
3.8.1
Gene Expression
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Mutagenic agents - exposure to them ca increase the rate of mutations e.g. ionising radiation, chemicals (Ethanol, Asbestos)
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Transcription Process
- Section of a DNA molecule (a single gene)
- DNA double helix unzips due to DNA helicase action. Hydrogen bonds between complementary bases break and the two polynucleotide strands separate.
- One strand acts as a template while the other is a coding strand. Free RNA nucleotides form H-bonds with exposed bases according to complementary base pairing rules.
- RNA polymerase forms phosphodiester bonds between RNA nucleotides to create a strand of RNA in a condensation reaction.
- In eukaryotes, pre-mRNA detaches from the template strand. The two DNA strands join back together by complementary base pairing and wind back into a helix.
Splicing
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Alternative splicing is two different ways to splice the same pre-mRNA to make two similar but different proteins e.g. Antibody gene
Translation Process
- Ribosome attaches to the start and second codon on the mRNA.
- Anticodon on the first tRNA binds to the complementary start codon on mRNA (H-bonds, complementary base pairing) bringing specific amino acids to ribosome.
- Anticodon on second tRNA binds...etc.
- ATP hydrolysis is required as a source of energy for the ribosome to form the peptide bond between amino acids.
- The ribosome moves along the mRNA to cover codon 2 and 3.
- The first tRNA is released. Anticodon on third tRNA binds ...etc.
The Genetic Code
Universal - In every organism, the same triplet codes for the same amino acid
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Effects of Mutation
- Mutation occurs (change in base sequence)
- This changes the order of mRNA bases in transcription, resulting in a different mRNA codon.
- This changes the tRNA anticodon complementary to the mRNA codon.
4a. This changes the amino acid incorporated into the primary structure of a protein or results in a premature stop codon.
4b. This does not change the amino acid incorporated into the primary structure of a protein due to the degenerate nature of the genetic code.
Types of mutation
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Inversion
Section of a chromosome detaches and re-attaches in the same position, but back to front
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Translocation
A sequence of bases in a section of the chromosome detaches from the chromosome and re-attaches to a different chromosome in a different place
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3.8.2.2
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Epigenetics
Epigenetics - heritable changes in the phenotype of organisms not as a result of DNA base sequence changes
Euchromatin - DNA loosely coiled around histone proteins (Not dense, appears lighter in colour)
Heterochromatin - DNA tightly coiled around histone proteins (dense, darker in colour)
Reduce Transcription
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Cause shape of promoter region to change, prevents transcription factors binding , this silences genes
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Increase Transcription
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Neutralises positive charges on histone proteins. The negative DNA can no longer wrap tightly and chromatin unwinds.
Unfolded genes allow gene expression, the genes are transcriptionally active
Chromosome - DNA coiled around histone proteins to form chromosomes. This is packed to form chromatin.
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3.8.2.1
Stem Cells
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They are capable of undergoing cell division (mitosis) to regenerate itself and produce daughter cells that are then able to specialise into different cell types
Totipotent
Divides repeatedly and differentiate into every cell type, therefore able to produce a full organism
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Specialised
A cell that has taken on a specific shape or structure in order to be able to perform a defined function within a tissue, organ or organism.
It only expresses the genes it requires to perform this function.
In many cases, they lose the ability to divide.
e.g. Motor neurone in adult human, heart muscle cell in adult human, gut epithelial cell in adult human
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3.8.2.3
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Benign Tumour
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Differentiated, as expected
Enclosed by a capsule, cells connected to each other, non-invasive
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Malignant Tumour
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Rapid growth, because division is uncontrolled
Larger nuclei, extra copies of chromosomes
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No capsule, no adhesive molecules
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Removal with surgery, chemotherapy and radiotherapy
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