scholarly journals The HERC1 ubiquitin ligase regulates presynaptic membrane dynamics of central synapses

2020 ◽  
Vol 10 (1) ◽  
Author(s):  
Mª Angeles Montes-Fernández ◽  
Eva Mª Pérez-Villegas ◽  
Francesc R. Garcia-Gonzalo ◽  
Leonardo Pedrazza ◽  
Jose Luis Rosa ◽  
...  
2011 ◽  
Vol 2 (1) ◽  
Author(s):  
Danming Tang ◽  
Yi Xiang ◽  
Stefano De Renzis ◽  
Jochen Rink ◽  
Gen Zheng ◽  
...  

Observations on the fine structure of synaptic and non-synaptic axoplasm in the spinal cord of the lamprey ammocoete ( Petromyzon marinus ) are described. Previous studies on this material revealed a close association between spherical vesicles and axoplasmic microtubules near central synapses, and observations were consistent with the suggestion that synaptic vesicles become detached from oriented microtubules in the focal clusters adjoining the presynaptic membrane across which transmitter release takes place. These observations have been extended to include axons containing non-spherical or ellipsoidal vesicles— possibly containing a transmitter chemically and functionally distinct from that in spherical synaptic vesicles. Structural cross-bridges between both microtubules and vesicle populations are now described; these are found not only in the vesicle concentrations bordering synaptic foci, but also in non-synaptic axoplasmic regions where sparsely distributed vesicles are found in association with microtubules. It is suggested that the bridging between vesicles and microtubules may reflect a mechanism for transport of the former—a possibility in accord with cumulative evidence of involvement of microtubules in rapid intracellular translocation in a variety of cells. It is proposed that arrival of excitation at a synaptic site is not only coupled with transmitter release across the axon plasma membrane, but that events at the cell membrane may in turn be coupled with a means of supplying vesicles to the synaptic locus. This hypothesis suggests that the synapse may rely on distant parts of the neuron, perhaps including the cell body, for materials involved in synaptic transmission.


Author(s):  
K. Jacobson ◽  
A. Ishihara ◽  
B. Holifield ◽  
F. Zhang

Our laboratory is concerned with understanding the dynamic structure of the plasma membrane with particular reference to the movement of membrane constituents during cell locomotion. In addition to the standard tools of molecular cell biology, we employ both fluorescence recovery after photo- bleaching (FRAP) and digitized fluorescence microscopy (DFM) to investigate individual cells. FRAP allows the measurement of translational mobility of membrane and cytoplasmic molecules in small regions of single, living cells. DFM is really a new form of light microscopy in that the distribution of individual classes of ions, molecules, and macromolecules can be followed in single, living cells. By employing fluorescent antibodies to defined antigens or fluorescent analogs of cellular constituents as well as ultrasensitive, electronic image detectors and video image averaging to improve signal to noise, fluorescent images of living cells can be acquired over an extended period without significant fading and loss of cell viability.


2015 ◽  
Vol 58 ◽  
pp. 83-100 ◽  
Author(s):  
Selena Gimenez-Ibanez ◽  
Marta Boter ◽  
Roberto Solano

Jasmonates (JAs) are essential signalling molecules that co-ordinate the plant response to biotic and abiotic challenges, as well as co-ordinating several developmental processes. Huge progress has been made over the last decade in understanding the components and mechanisms that govern JA perception and signalling. The bioactive form of the hormone, (+)-7-iso-jasmonyl-l-isoleucine (JA-Ile), is perceived by the COI1–JAZ co-receptor complex. JASMONATE ZIM DOMAIN (JAZ) proteins also act as direct repressors of transcriptional activators such as MYC2. In the emerging picture of JA-Ile perception and signalling, COI1 operates as an E3 ubiquitin ligase that upon binding of JA-Ile targets JAZ repressors for degradation by the 26S proteasome, thereby derepressing transcription factors such as MYC2, which in turn activate JA-Ile-dependent transcriptional reprogramming. It is noteworthy that MYCs and different spliced variants of the JAZ proteins are involved in a negative regulatory feedback loop, which suggests a model that rapidly turns the transcriptional JA-Ile responses on and off and thereby avoids a detrimental overactivation of the pathway. This chapter highlights the most recent advances in our understanding of JA-Ile signalling, focusing on the latest repertoire of new targets of JAZ proteins to control different sets of JA-Ile-mediated responses, novel mechanisms of negative regulation of JA-Ile signalling, and hormonal cross-talk at the molecular level that ultimately determines plant adaptability and survival.


Author(s):  
Leilani M. Chirino ◽  
Suresh Kumar ◽  
Mariko Okumura ◽  
David E. Sterner ◽  
Michael Mattern ◽  
...  

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