Enhancing the usefulness of artificial seeds in seed beetle model systems research

2020 ◽  
Vol 11 (12) ◽  
pp. 1701-1706
Author(s):  
Leslie A. Holmes ◽  
William A. Nelson ◽  
Markus Dyck ◽  
Stephen C. Lougheed
2018 ◽  
Vol 99 (11) ◽  
pp. e155
Author(s):  
Alejandro Zarate ◽  
Coralynn Long ◽  
Ellen Hada ◽  
Michael Juszczak ◽  
Michelle Smith ◽  
...  

Author(s):  
Nina Wale ◽  
Meghan A Duffy

Ever since biologists began studying the ecology and evolution of infectious diseases (EEID), laboratory-based ‘model systems’ have been important for developing and testing theory. Yet what EEID researchers mean by ‘model systems’ and what they want from them remains to be clearly delineated. This uncertainty holds back our ability to maximally exploit these systems, identify knowledge gaps, and establish effective new model systems. Here, we borrow a definition of model systems from the biomolecular sciences to assess how EEID researchers are (and are not) using ten key model systems. According to this definition, model systems in EEID are not being used to their fullest and, in fact, cannot even be considered to be model systems. Research using these systems consistently addresses only two of the three fundamental processes that underlie disease dynamics-transmission and disease, but not recovery. Further, studies tend to focus on only a few of the scales of biological organization that matter for disease ecology and evolution. Moreover, the field lacks an infrastructure to perform comparative analyses. We aim to begin a discussion of what we want from model systems, which would further progress toward a thorough, holistic understanding of EEID.


Author(s):  
K. Brasch ◽  
J. Williams ◽  
D. Gallo ◽  
T. Lee ◽  
R. L. Ochs

Though first described in 1903 by Ramon-y-Cajal as silver-staining “accessory bodies” to nucleoli, nuclear bodies were subsequently rediscovered by electron microscopy about 30 years ago. Nuclear bodies are ubiquitous, but seem most abundant in hyperactive and malignant cells. The best studied type of nuclear body is the coiled body (CB), so termed due to characteristic morphology and content of a unique protein, p80-coilin (Fig.1). While no specific functions have as yet been assigned to CBs, they contain spliceosome snRNAs and proteins, and also the nucleolar protein fibrillarin. In addition, there is mounting evidence that CBs arise from or are generated near the nucleolus and then migrate into the nucleoplasm. This suggests that as yet undefined links may exist, between nucleolar pre-rRNA processing events and the spliceosome-associated Sm proteins in CBs.We are examining CB and nucleolar changes in three diverse model systems: (1) estrogen stimulated chick liver, (2) normal and neoplastic cells, and (3) polyploid mouse liver.


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