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Intro
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LECTURE OUTLINE
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DNA IS THE MOLECULE THAT ENCODES THE BLUEPRINT OF LIFE
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AND YET GENOME SIZE DOES NOT PREDICT ORGANISM COMPLEXITY
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AND GENOME SIZE DOES NOT PREDICT GENE COUNT (CODING DNA)
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SO, WHAT FUNCTION DOES ALL OF THE NON-CODING DNA SERVE 7
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DYNAMIC REARRANGEMENT IN LIVE CELL GENOME ARCHITECTURE
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OPTICAL MICROSCOPY ENABLES US TO OBSERVE A LIVING CELL
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BUT DIFFRACTION LIMITS OBSERVATION OF DNA ORGANISATION
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SO, WHAT ASPECTS OF GENOME ARCHITECTURE CAN WE SEE ?
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BREAKTHROUGH COLLABORATION-PHYSICS CHEMISTRY BIOLOGY
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ADVENT OF SUPER-RESOLUTION - SEEING GENOME ARCHITECTURE
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SO, HOW DO WE GET AROUND DIFFRACTION WITH FLUORESCENCE
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WHAT DOES THIS MEAN FOR IMAGING GENOME ARCHITECTURET
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HOW CAN WE IMAGE LIVE CELL NANOSCALE GENOME DYNAMICS
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HISTONE FRET - REPORTS NUCLEAR WIDE NUCLEOSOME PROXIM..
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QUESTION? HOW DOES DNA REPAIR MACHINERY SENSE DNA DAMAGE
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NUCLEAR ARCHITECTURE FACILITATES REPAIR FACTOR NAVIGATIR
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LECTURE SUMMARY
Description:
Explore the fascinating world of DNA visualization in living cells through fluorescence techniques in this 53-minute lecture by Dr. Elizabeth Hinde. Discover how physics enables real-time observation of DNA network spatial reorganization, potentially serving as an epigenetic control layer for gene expression. Learn about the challenges of optical microscopy in observing DNA organization due to diffraction limits, and understand the breakthrough collaborations between physics, chemistry, and biology that led to super-resolution imaging. Delve into the intricacies of genome architecture, live cell nanoscale genome dynamics, and how nuclear architecture facilitates DNA repair factor navigation. This lecture, part of the University of Melbourne's Science Festival, offers insights into the complex relationship between genome size, organism complexity, and gene count, while highlighting the potential functions of non-coding DNA.

Glow in the Dark - Using Fluorescence to Observe DNA in a Living Cell

University of Melbourne
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