1 / 17

Unit 3: Interphase Nucleus

Unit 3: Interphase Nucleus. Heterochromatin. Nucleolus: site of ribosomal assembly and rRNA transcription. Heterochromatin : dark, condensed DNA that is transcriptionally inactive during interphase.

maya
Download Presentation

Unit 3: Interphase Nucleus

An Image/Link below is provided (as is) to download presentation Download Policy: Content on the Website is provided to you AS IS for your information and personal use and may not be sold / licensed / shared on other websites without getting consent from its author. Content is provided to you AS IS for your information and personal use only. Download presentation by click this link. While downloading, if for some reason you are not able to download a presentation, the publisher may have deleted the file from their server. During download, if you can't get a presentation, the file might be deleted by the publisher.

E N D

Presentation Transcript

  1. Unit 3: Interphase Nucleus

  2. Heterochromatin Nucleolus: site of ribosomal assembly and rRNA transcription Heterochromatin: dark, condensed DNA that is transcriptionally inactive during interphase. Nuclear Envelope: Contains a double membrane surrounding the nucleus. Contains nulear pores throughout. Euchromatin: lighter, transcriptionally active DNA Euchromatin Nuclear Envelope Nucleolus Interphase Nucleus

  3. Nucleolus Nucleoli are not bounded by a membrane. They are modified chromosomal loops that are transcriptionally active and involved in synthesis of rRNA. Three types of components: 1. DNA that is not actively synthesizing r-RNA. 2. RNA molecules in the process of rRNA synthesis 3. maturing ribosomal subunits.

  4. The Nuclear Pore • There are lots of nuclear pores • They have an elaborate structure • They are involved in the transport of RNAs and proteins.

  5. What goes In/Out In: Histone molecules Polymerases and other enzymes required for replication and regulation of replication Ribosomal proteins and other proteins (including snRNPs) that complex with newly formed transcripts. Out: Ribosomal subunits m-RNA Protein complexes. Only fully processed and spliced transcripts are allowed out of the nucleus.

  6. Transport into Nucleus Nucleoplasmin is a large protein with distinct head and tail regions.   The tails can be separated from the heads by limited proteolysis.  Colloidal gold is microscopic gold particles that can be made to a desired size and seen in the TEM.

  7. Steps of Import: 1. NLS protein combines with nuclear import receptor 2. The complex binds to a fibrils attached to the cytosol surface of the nucelar pore complex. 3. The fibril then bends 4. The protein is transferred to the central component of the nuclear pore complex. 5. The central component of the nuclear pore complex undergoes a conformational change that results in the protein being transferred to the nuclear side of the pore complex.

  8. CHROMATIN and CHROMOSOMESExperimental studies

  9. Chromatin Short region of DNA double helix Beads on a string form of chromatin This schematic drawing shows the orders of chromatin packing that give rise to the highly condensed mitotic chromosome. 30 nm chromatin fiber of packed nucleosomes Section of chromosome in an extended form Condensed section of chromosome Entire mitotic chromosome Each DNA molecule has been packaged into a mitotic chromosome that is 50,000 X shorter than its extended length

  10. Nucleosomes • The nucleosome consists of the core histone octamer surrounded by DNA wrapped around the outside of the proteins in approximately two turns per nucleosome. • This interaction forms a 'beads on a string structure' Histone molecules: 2 - H2A 2 - H2B 2 - H3 2 - H4

  11. What are Nucleases? • Enzymes that cleave nucleic acids (RNA or DNA). • Nucleases can be very specific,cutting the DNA or RNA between specific base pairs (targeting a specific nucleotide sequence). • A mixture of different nucleases can be used to create random cuts.

  12. Step 1 of Digestion • Chromatin is exposed to nuclease digestion. • The timing of the digestion is such that not every stretch of linking DNA is digested.

  13. Step 2 • The incomplete digestion of chromatin results in fragments of varying length, but in multiples of the length of one DNA/histone “bead on a string”. • For example, if 100 bp was involved in one “bead on a string”, this digestion will produce fragments of roughly 100, 200, 300 bp etc.

  14. Step 3 • Protein is removed to leave sections of naked DNA of varying length.

  15. Step 4 • The DNA fragments are separated via electrophoresis on an agarose gel. • The fragment lengths will be roughly multiples of the amount of DNA involved in one segment of the “beads on a string” model of histone-DNA packaging.

  16. Characterization of Nucleosomes • A mixture of different nucleases will cleave any exposed section of DNA indiscriminately. • Thus, a section of DNA that is protected by histones will not be digested. • Nucleases can be used to determine the length of DNA involved in one nucleosome, because there is a repeating pattern of histone protection. • Naked DNA, however, would produce a smear of many sized pieces of DNA until it is digested down to 1 base pair fragments.

  17. Example: Lane 1: Nuclease digestion of naked DNA. Lane 2: No nuclease digestion. Lane 3: Nuclease digestion of DNA associated with histones.

More Related