A complete set of repeat-depleted, PCR-amplifiable, human chromosome-specific painting probes

1999 ◽  
Vol 84 (3-4) ◽  
pp. 233-240 ◽  
Author(s):  
A. Bolzer ◽  
J.M. Craig ◽  
T. Cremer ◽  
M.R. Speicher
1999 ◽  
Vol 10 (7) ◽  
pp. 719-723 ◽  
Author(s):  
Leopoldo Iannuzzi ◽  
Giulia P. Di Meo ◽  
Angela Perucatti ◽  
Domenico Incarnato

Genomics ◽  
2004 ◽  
Vol 83 (2) ◽  
pp. 298-302 ◽  
Author(s):  
Liang Hu ◽  
Jonathan S.T Sham ◽  
Wai Mui Tjia ◽  
Yue-qiu Tan ◽  
Guang-xiu Lu ◽  
...  

2019 ◽  
Vol 116 (5) ◽  
pp. 1679-1685 ◽  
Author(s):  
Patrice S. Albert ◽  
Tao Zhang ◽  
Kassandra Semrau ◽  
Jean-Marie Rouillard ◽  
Yu-Hsin Kao ◽  
...  

Whole-chromosome painting probes were developed for each of the 10 chromosomes of maize by producing amplifiable libraries of unique sequences of oligonucleotides that can generate labeled probes through transcription reactions. These paints allow identification of individual homologous chromosomes for many applications as demonstrated in somatic root tip metaphase cells, in the pachytene stage of meiosis, and in interphase nuclei. Several chromosomal aberrations were examined as proof of concept for study of various rearrangements using probes that cover the entire chromosome and that label diverse varieties. The relationship of the supernumerary B chromosome and the normal chromosomes was examined with the finding that there is no detectable homology between any of the normal A chromosomes and the B chromosome. Combined with other chromosome-labeling techniques, a complete set of whole-chromosome oligonucleotide paints lays the foundation for future studies of the structure, organization, and evolution of genomes.


1996 ◽  
Vol 22 (1) ◽  
pp. 57-66 ◽  
Author(s):  
Fa-Ten Kao ◽  
Suhong Tong ◽  
Amy Whittier ◽  
Jingwei Yu

Author(s):  
Godfrey C. Hoskins

The first serious electron microscooic studies of chromosomes accompanied by pictures were by I. Elvers in 1941 and 1943. His prodigious study, from the manufacture of micronets to the development of procedures for interpreting electron micrographs has gone all but unnoticed. The application of todays sophisticated equipment confirms many of the findings he gleaned from interpretation of images distorted by the electron optics of that time. In his figure 18 he notes periodic arrangement of pepsin sensitive “prickles” now called secondary fibers. In his figure 66 precise regularity of arrangement of these fibers can be seen. In his figure 22 he reproduces Siegbahn's first stereoscopic electron micrograph of chromosomes.The two stereoscopic pairs of electron micrographs of a human chromosome presented here were taken with a metallurgical stage on a Phillips EM200. These views are interpreted as providing photographic evidence that primary fibers (1°F) about 1,200Å thick are surrounded by secondary fibers (2°F) arranged in regular intervals of about 2,800Å in this metanhase human chromosome. At the telomere the primary fibers bend back on themselves and entwine through the center of each of each chromatid. The secondary fibers are seen to continue to surround primary fibers at telomeres. Thus at telomeres, secondary fibers present a surface not unlike that of the side of the chromosome, and no more susceptible to the addition of broken elements from other chromosomes.


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