The purpose of this work was to elucidate the genetic fine structure of the central portion of mouse chromosome (Chr) 2. Seven Chr 2 congenic mouse strains [B10.PA(L)-pa we un at, B10.PA(L)-pa Aw, B10.PA(L)-we un at, B10.PA(J)-pa a, B10.FS-we Aw, B10.C-we Aw, and B10.YBR-a] were produced. Breeding s
Continued mapping of chromosome 2 genes
β Scribed by Ralph J. Graff; Vera Hauptfeld; Kevin Riordan; Michael Kurtz
- Publisher
- Springer-Verlag
- Year
- 1994
- Tongue
- English
- Weight
- 881 KB
- Volume
- 40
- Category
- Article
- ISSN
- 0093-7711
No coin nor oath required. For personal study only.
β¦ Synopsis
This report describes our continued efforts to elucidate the genetic fine structure of the central portion of the mouse chromosome (Chr) 2. Mice from our panel of 28 Chr 2 congenic strains were tested: 1) for the presence of the antigens which stimulate Chr 2-reactive lymphocyte clones in mixed lymphocyte reaction (MLR); 2) for the antigens of histocompatibility (H) genes H-42 a and H-45 a as determined by allograft rejection; and 3) for their ability to respond to the H-Y antigen in a cell-mediated lysis assay. The results obtained in this study have allowed additional mapping of immunologically involved Chr 2 genes. The gene encoding the antigen which stimulates lymphocyte clone 1Cll can be considered wholly different from other Chr 2 H genes on the basis of chromosomal recombination.
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