Skip to Main Content
Skip Nav Destination
ASTM Selected Technical Papers
Plants for Toxicity Assessment
By
W Wang
W Wang
1
Symposium Chairman and Editor
?
Illinois State Water Survey
?
Peoria, IL 61652
Search for other works by this author on:
JW Gorsuch
JW Gorsuch
2
Symposium Co-Chairman and Editor
?
Eastman Kodak Company
?
Rochester, NY 14652-3617
Search for other works by this author on:
WR Lower
WR Lower
3
Symposium Co-Chairman and Editor
?
University of Missouri
?
Columbia, MO 65203
Search for other works by this author on:
ISBN-10:
0-8031-1397-8
ISBN:
978-0-8031-1397-8
No. of Pages:
371
Publisher:
ASTM International
Publication date:
1990

Tradescantia paludosa (spiderwort) has been one of the classical materials for cytogenetic studies since the late 1930s, and it possesses a number of endpoints to measure genotoxicity. Cytogenetic and genetic endpoints include chromosome/chromatid aberrations in its mitotic cells of microspores, root meristems, pollen tubes; meiotic pollen mother cells and gene mutation in the cells of staminal hairs. Although sister chromatid exchange (SCE) was first discovered in the plant root meristem of Allium cepa, the SCE technique has not yet been developed for Tradescantia root tip cells. Based upon the principles and technical procedures to measure SCEs in other plant systems, a standard SCE protocol was developed for Tradescantia in this study. Unlike the other plant system, Tradescantia roots developed from stem cuttings were used for SCE analysis. The major steps of this protocol include: root initiation, 5-bromodeoxyuridine (5-BrdU) treatment, thymidine chasing, colchicine treatment, fixation, pectinase digestion, squashing the meristematic cells under the coverglass, removal of coverglass, treatment with Hoechst and sodium salt solutions, UV-light treatment, staining with Giemsa. Well prepared slides were photographed under 400X magnification and analyzed for SCE frequencies. In addition, the spontaneous SCE frequency of Tradescantia was compared with those of Vicia and Allium.

1.
Taylor
,
J. H.
, “
Sister Chromatid Exchanges in Tritium-Labeled Chromosomes
,”
Genetics
, Vol.
43
,
1958
, pp. 515–529.
2.
Korenberg
,
J. R.
and
Freedlender
,
E. F.
, “
Giemsa Technique for the Detection of Sister Chromatid Exchanges
,”
Chromosoma (Berl.)
, Vol.
48
,
1974
, pp. 355–360.
3.
Davidson
,
K. L.
,
Kaufman
,
E. R.
,
Daugherty
,
C. P.
,
Ouellette
,
A. M.
,
DiFolco
,
C. M.
, and
Latt
,
S. A.
, “
Induction of Sister Chromatid Exchange by BrdU is Largely Independent of the BrdU Content of DNA
,”
Nature
 0028-0836, Vol.
284
,
1980
, pp. 74–76.
4.
DuFrain
,
R.
and
Garrand
,
T. J.
, “
The Influence of Incorporated Halogenated Analogues of Thymidine on the SCE Frequencies in Human Lymphocytes
,”
Mutation Research
, Vol.
91
,
1981
, pp. 233–238.
5.
Ma
,
T. H.
, and
Harris
,
M. M.
In situ Monitoring of Environmental Mutagens
,” in
Hazard Assessment of Chemicals: Current Development
, Vol.
4
,
Academic Press
,
New York
,
1985
, pp. 77–106.
6.
Kihlman
,
B. A.
and
Kronborg
,
D.
, “
Sister Chromatid Exchanges in Vicia faba: I—Demonstration by a Modified FPG Technique
,”
Chromosoma
, Vol.
51
,
1975
, pp. 1–10.
7.
Scheid
,
W.
, “
Mechanism for Differential Staining of BrdU Substituted Vicia faba Chromosomes
,”
Experimental Cell Research
, Vol.
101
,
1976
, pp. 55–58.
8.
Cortes
,
F.
and
Anderson
,
H. C.
,
Analysis of SCEs on Vicia faba Chromosomes by a Simple Fluorescent Plus Giemsa Technique
,”
Hereditas
, Vol.
107
,
1987
, pp. 7–13.
9.
Schvartzman
,
J. B.
and
Cortes
,
F.
, “
Sister Chromatid Exchange in Allium cepa
,”
Chromosoma
, Vol.
62
,
1977
, pp. 119–131.
10.
Gutierrez
,
C.
,
Gonzalez-Gil
,
G.
, and
Hernandez
,
P.
, “
Analysis of Baseline BrdU-Dependent SCEs at Different BrdU Concentrations
,”
Experimental Cell Research
, Vol.
149
,
1983
, pp. 461–469.
11.
Wolff
,
S.
and
Perry
,
P.
, “
Differential Giemsa Staining of Sister Chromatids and the Study of Chromatid Exchanges without Autoradiography
,”
Chromosoma
, Vol.
48
,
1974
, pp. 341–353.
This content is only available via PDF.
You do not currently have access to this chapter.
Close Modal

or Create an Account

Close Modal
Close Modal