Investigation of genetic diversity and polyandry of Leptinotarsa decemlineata using X-linked microsatellite markers.

A panel of X-linked microsatellite markers was newly designed using the data from a previous sequencing project available in NCBI and used for a study of the Colorado potato beetle (CPB, Leptinotarsa decemlineata) X-haplotype variability. The analysis of scaffolds 49 and 61 (newly identified as fragments of CPB chromosome X) found ten high-quality markers, which were arranged in two PCR multiplexes and evaluated in both 420 CPB adults, collected from 14 localities of Czechia and Slovakia, and 866 larvae from five single-female families from two more Czech localities. Length polymorphisms found in 6 loci have predicted 192 potential X-haplotypes, however, only 36 combinations were detected in the adult males (N = 189), and seven additional ones in the larvae. The X-haplotypes were also generally unevenly distributed; five of the most frequent haplotypes were detected in 55% of males, 19 repeating up to ten-times in 38.7% of males and the remained 12 occurred uniquely in 6.3% of males. Bulk analysis of X-haplotypes dissimilarity indicated seven haplotype groups diversified by mutations and recombinations. Two haplotypes showed a distinctive regional distribution, which indicates an east-west disruption of CPB migration probably caused by different environments of localities in the South Bohemia region and Vysocina region. On the contrary, the results indicate a south-north migration corridor alongside the Vltava River. In the single-female families, from 6 to 13 distinct paternal haplotypes were detected, which proved and quantified a frequented polyandry in CPB.

Thyroid hormone responsiveness of the L1210 murine leukemia cell line.

The presence of saturable and high affinity 3,5,3'-triiodothyronine (T3) binding sites was demonstrated in L1210 murine leukemia cell nuclei. Scatchard analysis revealed one class of receptors for T3 with Ka = 2.187 x 10(9) l/mol and a maximum binding capacity (Bmax) of 3.96 fmol/10(6) cells. The effects of T3 on protein phosphorylation and growth rate of L1210 cells were investigated in a medium containing T3-depleted fetal calf serum. T3 was observed to be effective in enhancing protein phosphorylation (153.06% +/- 5.99 SD) compared to cells grown in the absence of T3 (81.49% +/- 13.50 SD). Moreover, in the presence of high T3 concentration (11.15 nmol/l) T3 was found to significantly increase the cell growth rate. In addition, the T3 receptor-associated alterations during the cell cycle, as measured by flow cytometry, suggest that the presence of T3 receptors becomes evident during the late G1 phase of the cell cycle, and T3 receptor numbers increase during the S phase. These results suggest that in in vitro conditions representing high T3 concentration, the number of L1210 leukemia cells may be increased by T3 via nuclear receptors. The L1210 leukemia cell line may serve as a convenient tool for in vitro studies of nuclear receptors and/or mechanism of action of T3. The binding affinity of T3 receptors is similar to that found in rat hepatocytes or human lymphocytes.

Distribution of triiodothyronine nuclear receptors during the cell cycle in mouse leukemia cells.

The process of the appearance of thyroid hormone receptors in the cell cycle was studied in mouse leukemia cells L1210. After cell synchronization by 2 mM thymidine for 12 h followed by 80 nM Colcemid for 4 h, the specific binding of triiodothyronine (T3) to its nuclear receptors was determined 3, 6, 9 and 12 h after release from the thymidine-Colcemid block. Three h after release from the block, [125I]T3 specific binding was 11.4 +/- 2.5% of a control value measured for an asynchronous population. An upward slope in progression of T3 nuclear receptors was found 6 h (32.3% +/- 4.5%), 9 h (47.8% +/- 5.2%) and 12 h (83% +/- 4.3%) after release from thymidine-Colcemid block. The data suggest that processes involving T3 receptor promotion in cell nuclei are operative within the late G1 and S phases of the cell cycle, and thus the increase in T3 receptor concentration in the nuclei is in a positive correlation with the number of cells in the S compartment of the cell cycle.