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FEATURES |
Department of Biology, Trinity University, San Antonio, TX 78212
Each quarter, Cell Biology Education calls attention to several Web sites of educational interest to the life science community. The journal does not endorse or guarantee the accuracy of the information at any of the listed sites. If you want to comment on the selections or suggest future inclusions, please send a message to E-mail: rblyston{at}trinity.edu. The sites listed below were last accessed on August 25, 2004.
Web learning resources for this issue focuses on chromosomes. The topic was chosen in remembrance of Professor Hewson Hoyt Swift, who passed away January 1, 2004, at the age of 83. Dr. Swift was one of the founders of the American Society of Cell Biology (ASCB). A brief accounting of Swift's life can be found at http://www.ascb.org/profiles/9303.html or at http://www-news.uchicago.edu/releases/04/040122.swift.shtml. As a graduate student in the late 1960s, I always made a point to attend Swift's presentations at the annual ASCB meetings, for it was the best way to keep up with developments in chromosome structure and packing.
| INTRODUCTION |
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The visualization of the chromosome is heavily dependent on how the structure is prepared for microscopy. Acid or basic and hypertonic or hypotonic preparation solutions can have a profound effect on the appearance of the chromosome. The difference in T.S. Painter's (1923) original reported human chromosome count of 48 to that of Tjio and Levan's (1956) count of 46 was attributed, in part, to preparation technique. For a history of the determination of the human chromosome number, please visit the Web site listed below for Bioscene, volume 22 (August 1996), and locate issue 2, page 3.
http://papa.indstate.edu/amcbt/volume_22/
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| CHROMOSOME PREPARATION |
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http://www.protocol-online.org/prot/Cell_Biology/Chromosome/index.html
This site was created in 1999 and is maintained by Longcheng Li of the University of California, San Francisco. Hundreds of different preparation protocols are organized and listed here. The chromosome section contains 29 protocols for the preparation and analysis of chromosomes and their parts. Chromosome preparation protocols were contributed from several sources, including the labs of Thomas Reid of the National Cancer Institute and Tim Mitchison of Harvard University. Also included are five undergraduate lab-based protocols from William Heidcamp of Gustavus Adolphus College in Minnesota. These protocols were excerpted from Heidcamp's well-regarded Cell Biology Lab Manual. One of the Heidcamp protocols is the fast preparation of chromosome smears from Drosophila salivary glands. Another is in a section called "Karyotype Analysis." In this protocol, different types of chromosome banding are discussed: A, G, R, and C. Different combinations of enzymes and stains can reveal specific parts or bands of chromosomes. The tested Heidcamp chromosome protocols are designed to support activities in an undergraduate cell biology class. Other protocols in Protocol Online give one an overview of the many sources of cells that can be processed in a number of ways to reveal chromosomes and their parts.
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| CHROMOSOME BANDING, CHROMOSOME PAINTING, AND FISH |
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Figures 1, 2, 3, provided by David Adler, demonstrate the transition between spread, karyotype, and idiogram with human chromosomes. The chromosomes seen here are of the G banding type. Explanations and illustrations of chromosomal abnormalities are provided. Fluorescence in situ hybridization (FISH) is also explained.
The FISH technique has provided many new approaches to identifying and understanding how chromosomes work. Hosted by the University of Bari, Italy, the Web site below provides a good overview of the technique of multicolor FISH used for karyotyping. The technique described is referred to as "Chromosomal Bar Coding" (Figure 4).
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| PLANT CHROMOSOMES |
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http://www.bafz.de/baz99_e/baz_orte/qlb/igk/cytogenetics.htm
Information in terms of handling plant chromosomes is covered in four sections at this site. The first deals with preparation and homogeneous staining, the second provides descriptions of staining for specific band markers, the third section gives examples of FISH procedures for single genes, and the last section describes quantitative image analysis of chromosome-specific features. Figure 5 is representative of imaging of single plant genes and their quantitative analysis.
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| THE DEPARTMENT OF ENERGY AND CHROMOSOMES |
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From the site above one can advance to the site below.
http://www.ornl.gov/sci/techresources/Human_Genome/home.shtml
Several pages branch from this page to extremely rich teaching and learning sources. One of these is the Gene Gateway.
http://www.ornl.gov/sci/techresources/Human_Genome/posters/chromosome/
The Gene Gateway describes itself in the following terms:
Scientists, enabled by the Human Genome Project, are churning out an unprecedented volume of data on human chromosomes and the tens of thousands of genes residing on them, many associated with genetic disorders. These data, and many Web sites on human genetic disorders, are freely accessible on the Internet. Gene Gateway, originally designed as a Web companion to the popular Human Genome Landmarks poster, is a collection of guides and tutorials designed to help students and other novice users get started with some of the resources that make these data available to the public.
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Download the Gene Gateway Workbook (PDF), a collection of five activities with screenshots and step-by-step instructions designed to introduce new users to genetic disorder and bioinformatics resources on the Web. Download the Gene Gateway Handout (PDF), a 2-page flyer describing this Web site.
These two files open the way to a rich source of teaching and learning information. (PDF stands for portable document format from Adobe Systems and the reader for the PDF files is available at no charge from http://www.adobe.com/products/acrobat/readstep2.html.)
Figure 6 is a sample of a workbook that provides five high-impact activities. The workbook uses screen shots on how to use significant bioinformatics tools from the following Web sites: OMIM, Gene Reviews, NCBI Map Viewer, Entrez Gene, Gene Bank, Swiss-Prot, Protein Data Bank, and Protein Explorer. The primer assumes that the reader is a first-time user. It is a really good way to get at this wealth of information.
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http://www.ornl.gov/sci/techresources/Human_Genome/posters/chromosome/chooser.shtml
The information gathered in Figure 7 has a very high teaching and learning value. This kind of genetic disorder information can be reached at the following URL.
http://www.ornl.gov/sci/techresources/Human_Genome/posters/chromosome/cftr.shtml
The DOE site requires a great deal of time to fully appreciate. It is well laid out but dense with information, as was the mind of Dr. Swift. A true giant of cell biology left us with his passing.
E-mail address: rblyston{at}trinity.edu.
| REFERENCES |
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Painter, T.S. (1923). Studies in mammalian spermatogenesis, II. The spermatogenesis of man. J. Exp. Zool.37 , 291-321.[CrossRef]
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