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Essential Molecular Biology (BIOC0007) Notes - Transcriptional Regulation and Translation £6.49   Add to cart

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Essential Molecular Biology (BIOC0007) Notes - Transcriptional Regulation and Translation

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Explore Essential Molecular Biology at UCL. Navigate the intricacies of Transcriptional Regulation and Translation in this specialized resource tailored for Year 2 students. Uncover the molecular orchestration governing gene expression. These notes offer a humanized academic guide, deepening your c...

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  • December 1, 2023
  • 16
  • 2021/2022
  • Lecture notes
  • Dr eleni makrinou
  • All classes
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sujansathiendran
Transcriptional Regulation and Translation – Summary
Transcriptional Regulation
 Regulation of Transcription
o Initiation of transcription
 Assembly of general transcription factors at promotor – basal transcription machinery
o Activation of transcription
 Additional transcription factors bind promotor upstream regulatory elements
o Activation of transcription at a distance – distal regulation
 Elements that regulate transcription from a further distance = enhancer regions and distal
regulation
 Not every gene has enhancer elements
 Combination of different regulatory elements – allows regulation of transcription
o Tissue-specific, spatial, and temporal control
 Regulation of a specific gene is coordinated to where and when it is needed – through
promotor-proximal elements and distal enhancers
 Regulating initiation of eukaryotic gene transcription
o General transcription factors (GTFs) + mediator
+ chromatin acting enzymes
 Transcriptional activators bind to
specific regions of the DNA (enhancer
regions)
 Helps attract RNA polymerase
to the start of transcription
 Further upstream from
promotor elements (TATA box)
 Bound by activator proteins
 Mediator complex interacts with
transcriptional activator proteins
 Causing communication between activator proteins + polymerase + GTFs  to
enhance level of transcription
 Interacts with enhancer regions bound by activator proteins to enhance the level of
transcription
 Chromatin acting enzymes – makes eukaryotic DNA more accessible
 Chromatin opens up
 DNA made more accessible for RNA polymerase II by chromatin re-modellers +
histone-modifying enzymes
o Allowing ability to regulate individual gene transcription – where and when its needed
 Tissue-specific gene expression
o Transcription of albumin gene
 Albumin gene
 Core promotor – proximal elements bind to core
promotor
 Control elements – upstream elements including enhancer region
o Expression of albumin in 2 tissue types
 Liver – transcription of albumin at a high
level
 Required activator proteins are
found in a high level in the liver
 Brain – transcription at albumin at a low
(basal) level

,Transcriptional Regulation and Translation – Summary
 Required activator proteins are found in a low level in the liver
o Achieved through availability of proteins in different tissue types
 Proteins that bind to upstream control elements = regulatory transcription factors
 Tissue specificity achieved through expression of correct combination of required activators
 Transcription factor domains – a region with its own structure and function
o DNA binding domain
 Recognises DNA binding site
o One or more activation (or repression) domains
 Affects what needs to be done to upregulate transcription
 Gene activation
o Hormone-dependent gene activation by dimeric nuclear receptors
 When cortisol is not in cell – receptor is retained in cytoplasm by inhibitor binding to ligand
binding domain
 When cortisol diffuses into the cell through plasma membrane – has a higher affinity to
ligand = replacing inhibitor  allowing accessibility into nucleus  DNA binding domain
binds to response elements  allowing activation domain to stimulate transcription of
target genes
 Transcription of protein encoding genes – highly regulated at different levels
o Initiation of basal level of transcription
 GTFs in PIC in eukaryotes
 Operons in prokaryotes
o Enhancement of basal transcription
 Activators in prokaryotes and eukaryotes
o Tissue specificity
 Presence of activators limited to certain tissues
o Processing of mRNA = pre-mRNA  mature mRNA = 5’ cap, 3’ poly A tail, removal of introns
 Epigenetics – another level of transcriptional regulation
o A series of reversible modifications to chromatin
 Chemical modifications that alter levels of transcription globally
 Chromatin changes can be inherited – by chromatin changes not DNA sequence changes
o Study of changes in regulation of gene activity and expression – independent of gene sequence
o Mechanisms
 DNA methylation – at the level of the DNA helix
 Histone modifications – DNA is condensed around histones forming chromatin
 Non-coding RNA (ncRNA)
 DNA methylation
o Addition of a methyl group to a cytosine on DNA
 Cytosines normally before guanine = CpG – p = phosphate between nucleotides
 One methyl group added per CpG
 CpG island = regions of the genome that contain a large number of CpG dinucleotide repeats
o Tagging specific points on the DNA molecule with a methyl group
 Controls X-chromosome inactivation and expression of imprinted genes – which are key
regulators in development
 Represses the transcription of repeated sequences + prevents relocation of transposable
elements  maintaining genomic stability
 Marks the bodies of active genes – influencing on splicing
 Regulates gene expression by repressing promotor activity
 In eukaryotes:
o Promotor hypermethylation (lots of methyl groups) = silences genes
o Promotor hypomethylation (lack of methyl groups) = activates genes
o Interactions from methylation

, Transcriptional Regulation and Translation – Summary
 Unmethylated DNA
 Has open conformation – which is more accessible for transcription factors
 Methylated DNA
 Physically impedes binding of transcription factors
 Methyl CpG binding proteins preferentially bind methylated DNA through their
methyl CpG binding domains (MBD)
o DNA methylated code is read by proteins that recognise regions of
methylated DNA = methyl-binding proteins with methyl binding domains
o Read the epigenetic code and act on it directly or recruit effector proteins
o Mechanisms of methylation
 Maintenance methylation
 Maintains methylation pattern already established on DNA
 Important during development
 Enzyme = DNMT1 = DNA methyltransferase 1
 Steps
o Before replication
 DNA is fully methylated at CpG dinucleotides
o During replication
 New DNA strands are synthesised without methyl group
o After replication
 Each new DNA molecule has methylation on one strand = hemi-
methylated
o Methyl transferase enzyme
 Hemi-methylated DNA is recognised by methyl-transferase enzyme
– has specificity for hemi-methylated DNA = adds methyl groups to
unmethylated strand
o Resulting in fully methylated DNA
 De novo methylation
 Establishment of new methylation patterns by de novo methyltransferases
 Enzymes = DNMT3a + DNMT3b = DNA methyltransferase 3a + 3b
o Directed to DNA by sequence specific DNA binding proteins
 Occurs during early development – after removal of methylation after fertilisation
 Imprinting
o In most genes – copies inherited from mother and father are equally expressed
o Genomic imprinting = epigenetic gene regulation that results in expression from a single allele in a
parent-of-origin dependent manner
 Achieved through different methylation patterns + use of non-coding RNA
 Maternal and paternally inherited alleles are differentially expressed
 Silenced allele = imprinted allele
o E.g. lgf2 gene
 Imprint is erased when making gametes  then re-established according to the sex of the
individual
 In eggs – imprints reset to maternal patterns even from genes from the father
 In sperm – imprints reset to paternal patterns even from genes from the mother
 Correct imprinting pattern is permanently established on zygote
o Imprinting disorders
 When methylation patterns are not maintained correctly – results in overexpression of one
or both alleles
 If mechanism effects expression – as there is only one active allele – there is nothing
to fall back on
 Imprinted genes are often clustered on the same chromosome

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