Complementation of Methylobacterium organophilum mutants affected in pyrroloquinoline quinone biosynthesis genes pqqE and pqqF by cloned Escherichia coli chromosomal DNA

The hybrid plasmid pBGT3, a derivative of pLA2917 containing a 7.8-kb fragment of Escherichia coli DNA, was found to complement pqqE and pqqF mutants of Methylobacterium organophilum, both impaired in PQQ biosynthesis. The cloned fragment of E. coli DNA did not hybridize with DNA fragments containing pqqE or pqqF previously cloned from M. organophilum. Yet, in M. organophilum mutants, expression of pqqE and pqqF genes from E. coli resulted in a PQQ production estimated at 9-16% of the production observed in M. organophilum wild-type. The growth rate in methanol medium of the complemented M. organophilum mutants was about 60% of that of the wild-type.     

GENETIC ANALYSIS OF SKULL SHAPE VARIATION AND MORPHOLOGICAL INTEGRATION IN THE MOUSE USING INTERSPECIFIC RECOMBINANT CONGENIC STRAINS BETWEEN C57BL/6 AND MICE OF THE MUS SPRETUS SPECIES

To assess the genetic basis of the skull shape variation and morphological integration in mice, we have used a tool based on the cross between the distantly related mouse species Mus spretus (SEG/Pas strain) and the laboratory strain C57BL/6 called interspecific recombinant congenic strains (IRCSs). The genome of each IRCS consists on average of 1.3% of SEG/Pas derived sequences, located on multiple chromosomes as small-sized, DNA segments. Quantitative trait loci (QTL) on the skull shape, separated into dorsal and ventral sides, were analyzed in 17 IRCSs by a Procrustes superimposition method using 3D landmarks. The shapes of 16 strains differed significantly from C57BL/6. Discrepancy in the QTLs effects was found between the dorsal side and the anterior region of the ventral side due to a differential effect of the SEG/Pas alleles on the skull shape. A comprehensive analysis of all allelic combinations of the BCG-66H strain showed strong epistatic interactions between SEG/Pas segment acting on both skull sides. Epistatic pleiotropy and covariation between sides were dependent in SEG/Pas alleles direction and contributed to the strong morphological integration between sides. Introduction of Mus spretus alleles in a C57BL/6 background induced strong morphological changes mostly in SEG/Pas alleles direction and provided evidence for high level of morphological integration.     

The recovery of spleen-seeking and lymph-node-seeking thymus subpopulations following cortisol administration

The administration of cortisol acetate depleted the population of spleen-seeking thymus cells to a greater extent than the population of lymph node-seeking thymus cells. While the proportion of lymph node-seeking thymus cells was increased following cortisol administration to about five times that found in the normal thymus, the number of lymph node-seeking cells in the atrophied thymus was reduced to about one-fifth of the number present in the thymus of untreated mice. Cortisol administration completely eliminated the small proportion of TL-positive cells present among the lymph node-seeking population, and drastically reduced the proportion of TL-positive spleen-seeking cells. The rate of recovery of the number of spleen-seeking thymus cells was much more rapid than that of the lymph node-seeking cells. The number of spleen-seeking cells increased significantly within 12 days after the administration of cortisol, and full recovery was evident by day 20. In contrast, the number of lymph node-seeking cells started to increase only 18 days after cortisol administration, and reached the level found in the normal thymus about 8 days later. The recovery of TL-positive lymph node-seeking cells paralleled the recovery of the TL-negative lymph node-seeking population rather than that of the TL-positive spleen-seeking population. Possible developmental interrelations between the spleen-seeking and lymph node-seeking populations of thymus cells are discussed.     

Evidence for a role of the cytoskeleton in the in vitro folliculogenesis of the thyroid gland of the fetal rat

Summary Thyrotropic hormone (TSH) or cAMP accelerate the formation of follicular cavities in the explanted thyroid gland of the 15-day-old rat fetus. Cytochalasin B or vinblastine and nocodazole or colchicine, which disorganize microfilamental and microtubular structures respectively, inhibit or completely block in vitro-induced folliculogenesis. Exposure of the thyroid tissue to lumicolchicine, a structural isomer of colchicine deprived of antimicrotubular activity, does not inhibit the activation of folliculogenesis induced by TSH. These results are strong evidence for the supposition that microfilaments and microtubules are involved in the TSH-stimulated mechanisms resulting in thyroid folliculogenesis. Folliculogenesis requires the integrity of both microfilaments and microtubules.