Julie Theriot (Stanford, HHMI) 3: Evolution of a Dynamic Cytoskeleton

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Science Communication Lab

Science Communication Lab

Күн бұрын

www.ibiology.org/cell-biology...
In Part 1 of her talk, Dr. Theriot explains how tiny, nanometer sized actin molecules can self-assemble into filaments that are hundreds of microns in length. These actin filaments are constantly growing and shrinking and this dynamic behavior allows a network of actin to generate enough force to move a cell forward. The intracellular bacterial pathogen Listeria monocytogenes uses actin polymerization to propel itself through the cytoplasm and to invade other cells. Many years of studies using Listeria have allowed Theriot and others to dissect the regulation of actin network growth in Listeria “comet tails” and at the leading edge of crawling cells.
In her second lecture, Theriot explains that fish keratocytes are an excellent system to study rapid cell motility. By labeling actin and myosin in keratocytes, Theriot and her colleagues were able to follow turnover of actin in the lamellipodium. Unexpectedly, they found that myosin II plays in important role in actin disassembly at the rear of the cell and asymmetric localization of myosin at the back of the cell appears to govern cell turning. Similar mechanisms of actin and myosin cooperation seem to drive rapid movement in both fish keratinocytes and human neutrophils.
It has been known since the early 1990s that bacteria have homologues of both actin and tubulin. In general, however, bacteria are much simpler than eukaryotes. In her final lecture, Theriot speculates about the factors that have evolved to allow eukaryotes to modify their cytoskeletons and build bigger, morphologically complex, multicellular organisms.
Speaker Biography:
Julie Theriot attended college at the Massachusetts Institute of Technology, graduating with degrees in Physics and Biology. She pursued graduate training at the University of California, San Francisco, earning her Ph.D. in Cell Biology in 1993. After four years as a Fellow at the Whitehead Institute for Biomedical Research, Theriot moved to Stanford University School of Medicine where she is currently a Professor of Biochemistry and of Microbiology and Immunology. Since 2008, Theriot has also been an Investigator of the Howard Hughes Medical Institute.
Theriot's research focuses on how interactions at the molecular level determine cell behavior, in particular, how cells change their shape or direction of movement. Theriot has received numerous awards for her work including fellowships from both the David and Lucile Packard Foundation and the John D. and Catherine T. MacArthur Foundation. She has also been recognized for her exceptional teaching.

Пікірлер: 20
@vastg5453
@vastg5453 4 жыл бұрын
The breath of knowledge and the clarity of logic are amazing. Thank you for the great lecture.
@Sigurjon543
@Sigurjon543 6 жыл бұрын
This was such an entertaining and informative lecture, your passion really shines through. Thank you!
@rubysu7098
@rubysu7098 3 жыл бұрын
This series of lectures are informative and thought-provoking. Thank you!
@StewartChaimson
@StewartChaimson 5 жыл бұрын
Amazingly great and fascinating lecture, maybe the best I've seen so far (out of hundreds)!
@giledgar1948
@giledgar1948 6 жыл бұрын
Dr. Theriot, You're terrific. I thoroughly appreciate your lectures.
@numericalcode
@numericalcode Жыл бұрын
Did not realize these discoveries were so recent
@davidkincade7161
@davidkincade7161 3 жыл бұрын
Great stuff! Thank you!
@cynocephalusw
@cynocephalusw 4 жыл бұрын
Great lectures. I learned a lot. To contribute to your riddle of nucleation, I think it‘s useful to take a few steps backwards to get a better sight. A theoretical abstraction, that makes sense on many, many stages of development is the so called „absolution“. An absolution occurs, when a ressource becomes ubiquitous. In our case it‘s the ubiquity of oxygen. This special ubiquity made it possible for an archaeon to incorporate a bacterium, that was able to use oxygen for generating an additional amount of ATP, allowing the cell not only growing in a Thiomargarita mode, but into the third dimension. The 1:1 relation of ATP production and outer cell surface was no more. Before the mitochondrial revolution, Myxobacteria developed a quite different way to solve this issue not by internalising auxiliary troops, but by externalising duties to their conspecifics in a distributed organism. So they were able to build up the largest genomes in the bacterial world. Myxobacteria also developed very special ways of social motility.
@VR_Wizard
@VR_Wizard 8 жыл бұрын
Did the bacteria in minute 29:17 pay windows to use its patented logo. If not they should get a good lawyer. ;)
@rickfearn3663
@rickfearn3663 4 жыл бұрын
Dear Dr. Theriot: Your presentation is like riding a magic carpet through the cytoplasm, speculating and wondering about the causes of such differences in cells. Imagining is what leads to creative and innovative new theories. Good luck to you and your work. Now.... about the flowers... do you need my address now or when I discover the special nucleotide bacterial motors?
@essentialsofbiology1643
@essentialsofbiology1643 4 жыл бұрын
Fascinating, thanks again. I think prokaryotes choose not to make Type B structures because they are just too dangerous to mix with your chromosomes. Think about the pulling forces exerted by microtubule shrinking, or the pushing forces exerted by nucleated F-actin polymerization. Or the forces exerted by processive motor protein walks. Long DNA molecules are fragile you know... if you had these things running around the bacterial cytosol, kiss the genome goodbye! Eukaryotes must have first evolved the nucleus, then gone to town with cytoskeleton. Then got big. This explanation is supported by the fact(?) that MreB and FtsZ filaments are always just running along under the plasma membrane. Maybe anchored to it? Test, make C crescentus mutant MreB that polymerizes normally but does not care where. Predict genomic instability!
@scottnineteen
@scottnineteen 2 жыл бұрын
I'd still want to keep an eye on them, I mean they just look like they're up to no good, hunched tubular lurkers.
@michaelmacdonald2907
@michaelmacdonald2907 4 жыл бұрын
What - that's it ? No season 2 ?! Don't leave me like this Don't break my heart It took me 40 years to find you . . . and now you're gone ?!!!
@dannichols6261
@dannichols6261 4 жыл бұрын
Are you thinking of: kzfaq.info/get/bejne/rbd5d5Wr0su7hIU.html ?
@scottnineteen
@scottnineteen 2 жыл бұрын
I think they try and very rarely do be semi multicelular thing and then get eaten, They're late is their problem
@propagandhi7159
@propagandhi7159 4 жыл бұрын
Perspicuous, Coherent, Compelling . . . say - you wanna go get a cup of coffee or something ?
@HereWasDede
@HereWasDede 2 жыл бұрын
What three people disliked this?
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