Linkage analyses using biochemical variants in mice. III. Linkage relationships of eleven biochemical markers

Hutton, John J.; Roderick, Thomas H.

doi:10.1007/bf00485782

Cited by 110 publications

(21 citation statements)

References 21 publications

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“…four-point backcross which will include the inversion and loci bf (buff), Id (retinal degeneration), and Bgm-_1_. The linkage of Pgm-1 and W (dominant spotting) was found by Hutton and Roderick (1970), and, although its direction from H is not certain, preliminary evidence suggests it is in the direction of kf· The data at this time indicate the inversion is beyond kf toward the end of the chromosome (Figure 3). Because this particular inversion forms rather short anaphase bridges, we believe the centromere must be located at the bf end of the chromosome.…”

Section: Characteristics Of Each Inversion In the Mouse Following Ismentioning

confidence: 86%

“…The data are summarized in Table 3 Most important about this region of the chromosome is that it contains two isozyme loci, both of which are in the inversion. Hutton and Roderick (1970) identified the linkage group and position of Id-1. found the linkage group of Dip-1 because of its linkage with Id-1.…”

Section: Characteristics Of Each Inversion In the Mouse Following Ismentioning

confidence: 99%

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RADIATION-INDUCED CHROMOSOMAL INVERSIONS IN MICE. Progress Report, December 1970--May 31, 1972.

Roderick¹

1972

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Section: Characteristics Of Each Inversion In the Mouse Following Ismentioning

confidence: 86%

Section: Characteristics Of Each Inversion In the Mouse Following Ismentioning

confidence: 99%

RADIATION-INDUCED CHROMOSOMAL INVERSIONS IN MICE. Progress Report, December 1970--May 31, 1972.

Roderick¹

1972

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“…The mapping was established using two markers, Mpi-1 and Mod-1, which had previously been localized on chromosome 9 (Hutton and Roderick, 1970;Nichols et al, 1973 . Preliminary results of a three-point cross involving ES-17, MPI-1, and ES-14 in 32 backcrosses (Bonhomme and yon Deimling, unpublished, 1981) Unlike the clustered esterase genes on chromosome 8, the three genes Es-13, Es-14, and Es-17 thus appear to be scattered over chromosome 9.…”

Section: Discussionmentioning

confidence: 99%

Esterase-17 (ES-17): Characterization and genetic location on chromosome 9 of a bis-p-nitrophenyl phosphate-resistant esterase of the house mouse (Mus musculus)

Otto

Deimling

1983

Biochem Genet

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Genetic variation of a new codominantly inherited esterase, designated ES-17, has been discovered in the house mouse using isoelectric focusing in polyacrylamide gels. The ES-17 A phenotype (three bands; isoelectric points, between pH 5.55 and pH 5.90) was found in C57BL/10Sn. LP/J possessed the Es-17B phenotype (three bands; isoelectric points, pH 5.05-5.55). ES-17 was present in all tissues examined, except for hemolysate and serum, and was most clearly expressed in the small intestine. Because of its reaction toward various substrates and inhibitors, ES-17 has tentatively been classified as acetyl esterase (EC 3.1.1.6). ES-17 was shown to be controlled by the structural locus Es-17, located on chromosome 9. From test-cross data, a gene order of Es-17-8.7 +/- 2.5 map units-Mpi-1-10.2 +/- 2.7 map units-Mod-1 was established.

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“…The structural gene for the hemoglobin | 3 chain, Hbb. is linked to the c locus in mouse (Popp, 1962 ;Hutton & Roderick, 1970), rat (Moutier et al, 1973a) and rabbit by about 6 cM. The linkage order in both rat and mouse is p -c -Hbb.…”

Section: Discussionmentioning

confidence: 99%

Protein polymorphisms in American deermice (Peromyscus) and genetic linkage homology

Dawson¹

1982

Acta Theriol.

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were backcrossed to deermice. The parents and backcross progeny were typed by gel electrophoresis for hemoglobin; serum albumin, transferrin, leucine amino peptidase, and esterases; kidney esterases; and liver alcohol dehydrogenase and malic dehydrogenase. Hemoglobin, malic dehydrogenase and some esterases did not differ between species stocks. Of 15 proteins classified in backcrosses, 9 were consistently variant between or within stocks. Inheritance of each protein segregated as a mendelian co-dominant system. Two probable cases of autosomal linkage were detected: Two kidney esterases were linked by 21 centimorgans and serum transferrin and leucine amino peptidase indicated linkage by 33 centimorgans.Linkage of esterase loci in Peromyscus is comparable to that in several other mammalian species, and probably represents phylogenetic homology. The significance of autosomal linkage conservation for evolution and development are discussed in the context of a proposed hypothesis.

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Linkage analyses using biochemical variants in mice. III. Linkage relationships of eleven biochemical markers

Cited by 110 publications

References 21 publications

RADIATION-INDUCED CHROMOSOMAL INVERSIONS IN MICE. Progress Report, December 1970--May 31, 1972.

RADIATION-INDUCED CHROMOSOMAL INVERSIONS IN MICE. Progress Report, December 1970--May 31, 1972.

Esterase-17 (ES-17): Characterization and genetic location on chromosome 9 of a bis-p-nitrophenyl phosphate-resistant esterase of the house mouse (Mus musculus)

Protein polymorphisms in American deermice (Peromyscus) and genetic linkage homology

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