Analysis of several key problems about the two linkage gene mapping of Neurospora crassa in genetics teaching

2012 ◽  
Vol 34 (1) ◽  
pp. 120-125
Author(s):  
Feng-Wei ZHANG ◽  
Shu-Liang SHI ◽  
Ning GU
1979 ◽  
pp. 377-394 ◽  
Author(s):  
U.L. RajBhandary ◽  
J.E. Heckman ◽  
S. Yin ◽  
B. Alzner-DeWeerd

Author(s):  
W. Bernard

In comparison to many other fields of ultrastructural research in Cell Biology, the successful exploration of genes and gene activity with the electron microscope in higher organisms is a late conquest. Nucleic acid molecules of Prokaryotes could be successfully visualized already since the early sixties, thanks to the Kleinschmidt spreading technique - and much basic information was obtained concerning the shape, length, molecular weight of viral, mitochondrial and chloroplast nucleic acid. Later, additonal methods revealed denaturation profiles, distinction between single and double strandedness and the use of heteroduplexes-led to gene mapping of relatively simple systems carried out in close connection with other methods of molecular genetics.


Author(s):  
Karen S. Howard ◽  
H. D. Braymer ◽  
M. D. Socolofsky ◽  
S. A. Milligan

The recently isolated cell wall mutant slime X of Neurospora crassa was prepared for ultrastructural and morphological comparison with the cell wall mutant slime. The purpose of this article is to discuss the methods of preparation for TEM and SEM observations, as well as to make a preliminary comparison of the two mutants.TEM: Cells of the slime mutant were prepared for thin sectioning by the method of Bigger, et al. Slime X cells were prepared in the same manner with the following two exceptions: the cells were embedded in 3% agar prior to fixation and the buffered solutions contained 5% sucrose throughout the procedure.SEM: Two methods were used to prepare mutant and wild type Neurospora for the SEM. First, single colonies of mutant cells and small areas of wild type hyphae were cut from solid media and fixed with OSO4 vapors similar to the procedure used by Harris, et al. with one alteration. The cell-containing agar blocks were dehydrated by immersion in 2,2-dimethoxypropane (DMP).


Pathology ◽  
1984 ◽  
Vol 16 (1) ◽  
pp. 16-21 ◽  
Author(s):  
Ronald J. Trent ◽  
P.E. Brock ◽  
J. Yakas ◽  
L.M. Trent ◽  
H. Kronenberg
Keyword(s):  

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