The Effect of Enucleation on Flagellar Regeneration in the Protozoon Peranema Trichophorum

1969 ◽  
Vol 4 (1) ◽  
pp. 171-178
Author(s):  
S. L. TAMM

A rotocompressor was used to enucleate the flagellate protozoon Peranema trichophorum at known stages in the mitotic cycle. This new enucleation technique, combined with recently devised methods for amputating the flagellum and recording its regeneration in single living cells, permitted the investigation of the role of the nucleus in flagellar regeneration at different cell ages. The flagellar regeneration capacity of an enucleate Peranema depended on the stage in the cell cycle when the nucleus was removed. Post-division enucleate cells regenerated about half the length reached by sham-operated controls, and at slower rates, while predivision enucleate cells regenerated flagella equally as well as the controls. Therefore, the nucleus is making an immediate contribution to flagellar regeneration early in the cell cycle, but not late in the cell cycle.

The Analyst ◽  
2013 ◽  
Vol 138 (14) ◽  
pp. 3891 ◽  
Author(s):  
Donna R. Whelan ◽  
Keith R. Bambery ◽  
Ljiljana Puskar ◽  
Don McNaughton ◽  
Bayden R. Wood

2020 ◽  
Author(s):  
Ying Feng ◽  
Yao Wang ◽  
Chen Yang ◽  
Ardalan Naseri ◽  
Thoru Pederson ◽  
...  

Epigenetic modifications play an essential role in chromatin architecture and dynamics. The role of epigenetic modification in chromatin organization has been studied by Hi-C from population cells, but imaging techniques to study their correlation and regulation in single living cells are lacking. Here we develop a CRISPR-based EpiGo (Epigenetic perturbation induced Genome organization) system to track epigenetic modification-mediated relocation, interaction or reorganization of genomic regions in living cells. EpiGo-KRAB is sufficient to induce the relocation of genomic loci to HP1α condensates and trigger genomic interactions. EpiGo-KRAB also triggers the induction of H3K9me3 at large genomic regions, which decorate on the surface of HP1α condensates possibly driven by phase separation.


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.


The Analyst ◽  
2021 ◽  
Author(s):  
Jia Liu ◽  
Dan Xie ◽  
Zhen Liu

Nuclear proteins are crucial in cells and are greatly linked to various biological functions. Abnormal expression of nuclear proteins is associated with many diseases ranging from inflammation to cancer. However,...


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