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Summary Lecture 6 - Posttranscriptional gene control and nuclear transport #2 $4.28
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Summary Lecture 6 - Posttranscriptional gene control and nuclear transport #2

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Lecture 6 - Posttranscriptional gene control and nuclear transport #2

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  • August 14, 2019
  • 6
  • 2017/2018
  • Summary
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Biochemistry and Molecular Biology II – Lecture 6: Posttranscriptional gene
control and nuclear transport #2 – Lecture by Ger Pruijn
08-05-2018

Nuclear speckles: areas with the highest concentration of splicing factors.

There are two types of enhancers:
1. On DNA-level
2. On RNA-level (exon-junction complex)

Alternative splicing: splicing more up- or downstream as normally (3’ or 5’ end)
Alternative splicing can result in many mRNAs from a single gene and can be
regulated in a tissue-specific manner.

Alternative splicing is regulated by RNA-binding proteins (Rbp’s).

Risks of alternative splicing:
- Frameshift can occur, leading to other genes and thus proteins.
- Complete exons can be skipped.

Depending on the position of the start codon, 5’ end splicing can affect the protein to
be synthesized (or not).




Alternative polyadenylation: does not affect the protein to be synthesized, because
the stop-codon lies in front (upstream) of the poly(A)-site.

Not all alternatively processed mRNAs are functional (NMD).

, There are many important consequences of alternative splicing, e.g. sexual
differentiation in Drosophila – determining the gender:




Skipping exon 3  female Drosophila.
Including exon 3  male Drosophila.

*The red line in exon 3 is caused by a nonsense mutation, leading to a premature
stop-codon  causing the resulting protein to be abnormally shortened.

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