DNA Content and DNA-Based Centromeric Index of the 24 Human Chromosomes

Science ◽  
1973 ◽  
Vol 179 (4078) ◽  
pp. 1126-1129 ◽  
Author(s):  
M. L. Mendelsohn ◽  
B. H. Mayall ◽  
E. Bogart ◽  
D. H. Moore ◽  
B. H. Perry
1966 ◽  
Vol 5 (3-4) ◽  
pp. 223-242 ◽  
Author(s):  
M.L. Mendelsohn ◽  
T.J. Conway ◽  
D.A. Hungerford ◽  
W.A. Kolman ◽  
B.H. Perry ◽  
...  

1974 ◽  
Vol 22 (7) ◽  
pp. 554-560 ◽  
Author(s):  
MORTIMER L. MENDELSOHN ◽  
DEBORAH E. BENNETT ◽  
ELLIOT BOGART ◽  
BRIAN H. MAYALL

A density-oriented semiautomatic method to estimate centromeric index is described and tested on 4611 human chromosomal images. Chromosomes are stained for deoxyribonucleic acid with gallocyanin-chrome alum and their optical density is recorded by a digital scanning microscope. Shape information in the chromosome boundary leads to a provisional centromeric position. The chromosome is divided into strips 0.25-0.35 µm wide paralleling the centromere. Optical density is integrated within each strip, strips are assembled into a density profile and the definitive centromere is located at the major local minimum in the profile. Centromeric index (large arm:total) is based on optical density or area. A test set of 4611 chromosomal images is based on over 2500 chromosomes (56 metaphase cells from six individuals) and excludes overlapped and excessively bent chromosomes. The program fails in 1.2% of the test images. Standard deviation within chromosome groups of centromeric index based on density is 0.024 and replication error is 0.016. Systematic differences between area-based and density-based measurements are observed and interpreted.


1990 ◽  
Vol 85 (1) ◽  
pp. 41-48 ◽  
Author(s):  
Gert A. Boschman ◽  
Wim Rens ◽  
Eric Manders ◽  
Carel van Oven ◽  
Gerrit W. Barendsen ◽  
...  

1986 ◽  
Vol 41 (1) ◽  
pp. 14-21 ◽  
Author(s):  
P. Harris ◽  
E. Boyd ◽  
B.D. Young ◽  
M.A. Ferguson-Smith

Author(s):  
Fred Eiserling ◽  
A. H. Doermann ◽  
Linde Boehner

The control of form or shape inheritance can be approached by studying the morphogenesis of bacterial viruses. Shape variants of bacteriophage T4 with altered protein shell (capsid) size and nucleic acid (DNA) content have been found by electron microscopy, and a mutant (E920g in gene 66) controlling head size has been described. This mutant produces short-headed particles which contain 2/3 the normal DNA content and which are non-viable when only one particle infects a cell (Fig. 1).We report here the isolation of a new mutant (191c) which also appears to be in gene 66 but at a site distinct from E920g. The most striking phenotype of the mutant is the production of about 10% of the phage yield as “giant” virus particles, from 3 to 8 times longer than normal phage (Fig. 2).


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