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Two closely linked genes in the mouse

Published online by Cambridge University Press:  14 April 2009

H. Grüneberg  and
G. M. Truslove
H. Grüneberg
Affiliation:
Medical Research Council Group for Experimental Research in Inherited Diseases, University College, London
G. M. Truslove
Affiliation:
Medical Research Council Group for Experimental Research in Inherited Diseases, University College, London
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(1) In heterozygous condition, the gene for Patch (symbol Ph) produces spotting with sharply defined pigmented and white areas. The extent of the spotting is under the control of the genetic background.

(2) The Ph/Ph homozygote is inviable and dies before birth. In 9-day embryos, clear liquid is found flanking the notochord; in addition, there may be excessive amounts of liquid in the pericardium, the circulation, the tissues, and under the epidermis. The more extremely affected Ph/Ph embryos die at about 10 days. About one-third survive to later stages of pregnancy. Such ‘cleft-face’ embryos have a large bleb of liquid in the middle of the face which interferes mechanically with the formative movements of the nose and palate, and many subepidermal blebs elsewhere.

(3) Ph is closely linked to the gene for dominant spotting with macrocytic anaemia (W, Wv) in linkage group III, the crossover percentage being 0·077. There is a striking interaction in the double heterozygote Ph + / + Wv which is almost white, but nearly equally striking interactions occur with other spotting genes (s, bt and Miwh).

(4) By itself, Ph has no detectable effect on the coat colour, but in the double heterozygote with Wv, it slightly increases the dilution effect of the latter in the regions which remain pigmented. Similarly, Ph by itself has no appreciable effect on the red-blood picture of 13–14-day-old animals, but in the double heterozygote with Wv, it probably slightly increases the mild macrocytic anaemia produced by that gene. It remains unknown whether the Ph/Ph homozygote has an effect on the blood. Unlike W/W and Wv/Wv, Ph/Ph has no appreciable effect on the primordial germ cells.

(5) The relationship between Ph and the W-series is discussed.

Information

Type
Research Article
Information
Genetics Research , Volume 1 , Issue 1 , February 1960 , pp. 69 - 90
Copyright
Copyright © Cambridge University Press 1960

References

REFERENCES

Auerbach, R. (1954). Analysis of the developmental effects of a lethal mutation in the house mouse. J. exp. Zool. 127, 305–330.CrossRefGoogle Scholar
Bennett, D. (1956). Developmental analysis of a mutation with pleiotropic effects in the mouse. J. Morph. 98, 199–234.CrossRefGoogle Scholar
Bonnevie, K. (1934). Embryological analysis of gene manifestation in Little and Bagg's abnormal mouse tribe. J. exp. Zool. 67, 443–520.CrossRefGoogle Scholar
Bonnevie, K. (1945). Hereditary hydrocephalus in the house mouse. III Manifestation of the hy-mutation in embryos 9–11 days old, and younger. Skr. norske VidenskAkad., I. Mat.-Naturv. Kl., 1944, No. 10, pp. 60.Google Scholar
Carter, T. C. (1955). The estimation of total genetical map lengths from linkage test data. J. Genet. 53, 21–28.Google Scholar
Dunn, L. C. (1956). Analysis of a complex gene in the mouse. Cold Spr. Harb. Symp. quant. Biol. 21, 187–95.CrossRefGoogle Scholar
Forsthoefel, P. F. (1958). The skeletal effects of the luxoid gene in the mouse, including its interactions with the luxate gene. J. Morph. 102, 247–287.CrossRefGoogle Scholar
Grüneberg, H. (1937). Gene doublets as evidence for adjacent small duplications in Drosophila. Nature, Land., 140, 932.CrossRefGoogle Scholar
Grüneberg, H. (1939). Inherited macrocytic anemias in the house mouse. Genetics, 24, 777–810.CrossRefGoogle ScholarPubMed
Grüneberg, H. (1942). Inherited macrocytic anaemias in the house mouse. II. Dominance relationships. J. Genet. 43, 285–293.CrossRefGoogle Scholar
Mintz, B. & Russell, E. S. (1957). Gene-induced embryological modifications of primordial germ cells in the mouse. J. exp. Zool. 134, 207–238.CrossRefGoogle ScholarPubMed
Morgan, W. C. (1950). A new tail-short mutation in the mouse whose lethal effects are conditioned by the residual genotype. J. Hered., 41, 208–215.CrossRefGoogle Scholar
Rawles, M. E. (1947). Origin of pigment cells from the neural crest in the mouse embryo. Physiol. Zool., 20, 248–266.CrossRefGoogle ScholarPubMed
Sarvella, P. A. & Russell, L. B. (1956). Steel, a new dominant gene in the house mouse with effects on coat pigment and blood. J. Hered. 47, 123–8.CrossRefGoogle Scholar
Truslove, G. M. (1952). Genetical studies on the skeleton of the mouse. V. ‘Interfrontal’ and ‘parted frontals’. J. Genet., 51, 115–22.CrossRefGoogle Scholar