Identification and genetic mapping of the murine gene and 20 related sequences encoding chromosomal protein HMG-17

HMG-17 is an abundant, nonhistone chromosomal protein that binds preferentially to nucleosomal core particles of mammalian chromatin. The human gene for HMG-17 has been localized to Chromosome (Chr) 1p, but the murine gene has not been previously mapped. Here we identify the murine functional gene, Hmg17, from among more than 25 related sequences (probably processed pseudogenes) and show that it is located on mouse Chr 4, in a region known to have conserved linkage relationships with human Chr 1p. We also report the map locations of 20 additional Hmg17-related sequences on mouse Chrs 1, 2, 3, 5, 7, 8, 9, 13, 15, 16, 17, 18, and X. The multiple, dispersed members of the Hmg17 multigene family can be detected efficiently with a single cDNA probe and provide useful markers for genetic mapping studies in mice

Genetic mapping of the murine gene and 14 related sequences encoding chromosomal protein HMG-14.

The high-mobility-group chromosomal protein HMG-14 preferentially binds to nucleosomal core particles of mammalian chromatin and may modulate the chromatin configuration of transcriptionally active genes. The human gene for HMG-14 has been localized to the Down syndrome region of Chromosome (Chr) 21 and may be involved in the etiology of this syndrome. Here we show, by means of genetic linkage analysis of interspecific and intersubspecific backcross mice, that the murine functional gene, Hmg14, is located on the distal end of mouse Chr 16, a region known to have conserved synteny with human Chr 21. In addition to the functional gene for HMG-14, both human and mouse genomes contain many related sequences that are probably processed pseudogenes. Here we map the locations of 14 Hmg14-related sequences in two mouse genomes. The 14 mapped loci are widely dispersed on ten chromosomes (Chrs 3, 5, 7, 9, 11, 12, 16, 17, 19, and X) and can be detected efficiently with a single cDNA probe. Thus, the Hmg14 multigene family is well suited to serve as genetic markers for other linkage studies in mice

Donor-impurity related binding energy and photoinization cross-section in quantum dots: electric and magnetic fields and hydrostatic pressure effects

We have studied the behavior of the binding energy and photoionization cross-section of a donor-impurity in cylindrical-shape GaAs-Ga0.7Al0.3As quantum dots, under the effects of hydrostatic pressure and in-growth direction applied electric and magnetic fields. We have used the variational method under the effective mass and parabolic band approximations. Parallel and perpendicular polarizations of the incident radiation and several values of the quantum dot geometry have also been considered. Our results show that the photoionization cross-section growths as the hydrostatic pressure is increased. For parallel polarization of the incident radiation, the photoionization cross-section decreases when the impurity is shifted from the center of the dot. In the case of perpendicular polarization of the incident radiation, the photoionization cross-section increases when the impurity is shifted in the radial direction of the dot. For on-axis impurities the transitions between the ground state of the impurity and the ground state of the quantum dot are forbidden. In the low pressure regime (less than 13.5 kbar) the impurity binding energy growths linearly with pressure, and in the high pressure regime (higher than 13.5 kbar) the binding energy growths up to a maximum and then decreases. Additionally, we have found that the applied electric and magnetic fields may favor the increase or decrease in binding energy, depending on the impurity position