scholarly journals The induction of dominant lethal mutations in rats and mice with triethylenemelamine (TEM)

1960 ◽  
Vol 1 (3) ◽  
pp. 381-392 ◽  
Author(s):  
A. J. Bateman

1. TEM resembles X-rays in inducing dominant lethal mutations in the sperm of rats and mice and sterilizing type B spermatogonia. Beyond this, however, there are several important differences.2. The relative ease with which TEM and X-rays affect sperm and spermatogonia varies greatly. The X-ray dose which produces 50% dominant lethals in sperm (500 rad) sterilizes spermatocytes and type B spermatogonia, and has such a drastic effect on type A spermatogonia that recovery of fertility is delayed for 2½ months. The TEM dose which produces the same mutation rate in sperm (0·1 mg./kg. rat) has no detectable effect on pre-meiotic stages. Even 1 mg./kg. only sterilizes the most sensitive stage, type B spermatogonia.3. Taking immature sperm as the standard, mature sperm are more sensitive to X-rays, but less sensitive to TEM, and early spermatids, the most sensitive stage to X-ray-induced dominant lethals, are highly resistant to TEM.4. Spermatocytes, in which X-rays yield a mutation rate equal to immaturesperm, are highly resistant to TEM.5. To produce the same mutation rate in immature sperm, mice require twice as much TEM as the rat in mg./kg., though approximately the same X-ray dose.6. In contrast to mid-stage rat spermatids, which are the most sensitive stage to TEM, mouse mid-stage spermatids are resistant.

Genetics ◽  
1974 ◽  
Vol 77 (4) ◽  
pp. 741-752
Author(s):  
W M Generoso ◽  
W L Russell ◽  
Sandra W Huff ◽  
Sandra K Stout ◽  
D G Gosslee

ABSTRACT Genetic damage by ethyl methanesulfonate (EMS) in male mice was measured at doses ranging from 50 to 300 mg/kg with dominant-lethal mutations and reciprocal translocations as endpoints. No appreciable increase in dominant-lethal mutations was detected following a dose of 100 mg/kg. Dominant lethals induced by EMS were convincingly detected only after a dose of 150 mg/kg, but in the translocation experiment an increase in the genetic effect was detectable at the 50 mg/kg dose. It is likely that dominant lethals had also been induced at the 50 and 100 mg/kg doses, but were not detected due to the relative insensitivity of the dominant%lethal procedure. Thus, for detection of low levels of EMS-induced chromosome breakage, translocations are a much more reliable endpoint than are dominant-lethal mutations. A procedure for large-scale screening of induced translocations is described.—The dominant-lethal dose-response curve, plotted on the basis of living embryos as a percentage of the control value, is clearly not linear as it is markedly concave downward. Similarly, the translocation dose-response curve showed a more rapid increase in the number of translocations with dose than would be expected on the basis of dose-square kinetics. It is clear for both of these endpoints that the effectiveness of EMS in inducing chromosome breakage is proportionately much lower at low doses.


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