Changes in the distribution of labeled retinal ganglion cells after an implant of DiI into the optic nerve in the chick embryos

Changes in the distribution of retinal ganglion cells (RGCs) were studied using the retrograde labeling of DiI in chicks and chick embryos. The small retinal area filled with labeled RGCs was observed in the retinal fundus on E8. The labeled retinal area expanded radially toward the peripheral retina as the retina grew, and finally occupied a whole retina by P1. The temporal retina was labeled more rapidly than in the nasal retina. The observed-increasing rate of the labeled area was corrected with the growing rate of the retina. Consequently, the corrected-increasing rate of the labeled area was estimated to be about 390% between E8 and E11, and 20-50% after E11. This means that spreading speed of the maturated RGCs lowered until 1/10-1/20 after E11.     

Identification of rRNA gene loci in the wild mouse (Mus musculus molossinus) captured at Hachioji, Tokyo

Mus musculus (M. m.) molossinus has been considered an independent subspecies of Mus musculus. To elucidate the evolutional origin of this subspecies, we carried out double-color FISH using 18s-28s ribosomal DNA and mouse chromosome paint probes. Among eleven rDNA loci detected, five loci on chromosomes 12, 15, 16, 18 and 19 were common to both Mus musculus (M. m.) musculus and M. m. molossinus and the other six loci, on chromosomes 1, 5, 10, 11, 13 and 17, were characteristic in M. m. molossinus. As M. m. molossinus is thought to originate from a hybrid between ancestral colonies of M. m. musculus and Mus musculus castaneus, we supposed that these six rDNA loci might have evolved after geographical isolation of the ancestral hybrid animals from M. m. musculus and M. m. castaneus.     

Mapping of rRNA gene loci in the mice, Mus musculus molossinus (Japan) and Mus musculus musculus (Russia) by double color FISH

Ribosomal RNA gene (rDNA) loci of Russian Mus musculus musculus and of Japanese Mus musuculus molossinus were mapped by double color FISH. The total number of rDNA loci was varied from 5 to 12, although the loci on chromosomes 12, 15, 16, 18, and 19 were common to all mice examined. Instead, polymorphisms of the rDNA loci were found on chromosomes 1, 5, 8, 9, 10, 11, 13 and 17. The novel rDNA loci of M. m. musculus were found in Nov/TUA strain on chromosomes 8 and 17. These observations, together with those of previous reports, suggest that the rDNA loci of Mus musculus species are in the evolutionary process of further translocation to other chromosomes.     

Effects of porcine leptin receptor gene polymorphisms on backfat thickness,fat area ratios by image analysis,and serum leptin concentrations in a Duroc purebred population

The leptin receptor (LEPR) gene is considered a candidate gene for fatness traits. It is located on SSC 6 in a region in which quantitative trait loci (QTLs) for backfat thickness (BF), fat area ratios, and serum leptin concentration (LEPC) have previously been detected in a Duroc purebred population. The objectives of the present study were to identify porcine LEPR polymorphisms and examine the effects of LEPR polymorphisms on fatness traits in this same population. The Duroc pigs (226 to 953 pigs) were evaluated for BF, fat area ratios using image analysis, and LEPC. A total of seven single nucleotide polymorphisms (SNPs) in the full‐length LEPR coding region were identified in pigs from the base population. Four non‐synonymous SNPs of the LEPR gene and 15 microsatellite markers on SSC 6 were then genotyped in all pigs. During candidate gene analysis, we detected significant effects of the non‐synonymous SNP c.2002C>T in exon 14 on all traits. In fine mapping analysis, significant QTLs for BF, fat area ratios, and LEPC were detected near the LEPR gene in the same region. These results indicated that the c.2002C>T SNP of LEPR has a strong effect on BF, fat area ratios and LEPC.     

Urinary albumin and transferrin as early diagnostic markers of chronic kidney disease

Feline renal diseases are increasingly noted in veterinary practice. It is important to diagnose and identify the pathological basis of renal dysfunction accurately at an early stage, but there are only a few reports on this area in clinical veterinary medicine. We investigated the efficacy of measurement of urinary albumin (u-Alb) and urinary transferrin (u-Tf) for early diagnosis using 5-µl urine samples collected noninvasively by catheterization from normal (IRIS stage I) cats and cats with stage I chronic kidney disease (CKD). The u-Alb levels in normal and stage I CKD cats were 6.0 ± 4.5 and 11.2 ± 8.4 mg/dl, respectively, and the u-Tf levels were 0.09 ± 0.42 and 0.52 ± 0.79 mg/dl, respectively. Based on ROC curve analysis, the sensitivity and specificity of u-Alb and u-Tf were higher than those of the currently used biomarker, the plasma creatinine level. The sensitivity of u-Alb was higher than that of u-Tf, whereas the specificity of u-Tf was higher than that of u-Alb. The validity of the threshold albumin level (20 mg/dl) was confirmed by measurements using SDS-PAGE. Since leakage of u-Tf in urine precedes leakage of u-Alb, inclusion of u-Tf in biochemistry tests may be appropriate for IRIS staging as a diagnostic marker of early diagnosis of renal disorder in cats.     

Effect of the amelioration of soil acidity and continuous cropping of cruciferous vegetables on the incidence of clubroot disease and resting spore density in soil

pp. 891–896
In order to elucidate the effect of converter furnace slag applied as a liming amendment and continuous cropping of Qing gin cai ( Brassicae chinensis L.) or leaf daikon ( Raphanus sativus ) on the incidence of clubroot disease and the resting spore density in soil, pot cultivation tests were carried out. In the pot tests, pH(H₂O) was 5.2–6.1 in the non-application pot, and 7.1–7.6 in the pots receiving an application of converter furnace slag.
A significant incidence of club-root disease was apparent in the non-application pots of Qing gin cai . The resting spore density in the soils decreased soon after harvesting, but then increased after mixing the infected roots and soils.
On the other hand, the incidence of the disease was suppressed significantly, in application pots of continuously cropped Qing gin cai . Furthermore, the resting spore density in these soils decreased with repeated cultivation.
These results agreed well with the results from field cultivation tests that the authors have already reported. Macfarlane has reported that the suppression mechanism of clubroot disease brought about by the amelioration of soil acidity is effected through the inhibition of resting spore germination.
In this study, the decrease of resting spores density was associated with the cultivation of Qing gin cai under conditions of high soil pH. From these results, it is concluded that the suppression mechanism is caused by some phenomenon that occurs after the primary zoospore is infected with the root hair.
Until now, avoidance of continuous cropping of susceptible cruciferous vegetables was promoted as one of the most fundamental countermeasures for the control of clubroot disease. However, continuous cropping of suceptible cruciferous vegetables will be a useful technique to decrease resting density specifically under conditions of high soil pH.     

Genetic basis of multiple resistance to the brown planthopper (Nilaparvata lugens St?l) and the green rice leafhopper (Nephotettix cincticeps Uhler) in the rice cultivar ‘ASD7’ (Oryza sativa L. ssp. indica)

The rice cultivar ASD7 (Oryza sativa L. ssp. indica) is resistant to the brown planthopper (BPH; Nilaparvata lugens Stål) and the green leafhopper (Nephotettix virescens Distant). Here, we analyzed multiple genetic resistance to BPH and the green rice leafhopper (GRH; Nephotettix cincticeps Uhler). Using two independent F₂ populations derived from a cross between ASD7 and Taichung 65 (Oryza sativa ssp. japonica), we detected two QTLs (qBPH6 and qBPH12) for resistance to BPH and one QTL (qGRH5) for resistance to GRH. Linkage analysis in BC₂F₃ populations revealed that qBPH12 controlled resistance to BPH and co-segregated with SSR markers RM28466 and RM7376 in plants homozygous for the ASD7 allele at qBPH6. Plants homozygous for the ASD7 alleles at both QTLs showed a much faster antibiosis response to BPH than plants homozygous at only one of these QTLs. It revealed that epistatic interaction between qBPH6 and qBPH12 is the basis of resistance to BPH in ASD7. In addition, qGRH5 controlled resistance to GRH and co-segregated with SSR markers RM6082 and RM3381. qGRH5 is identical to GRH1. Thus, we clarified the genetic basis of multiple resistance of ASD7 to BPH and GRH.     

Decomposition patterns of leaf litter of seven common canopy species in a subtropical forest： dynamics of mineral nutrients

Dynamical patterns of mineral elements during decomposition processes were investigated for seven common canopy species in a subtropical evergreen broad-leaved forest by means of litterbag technique over 2 years. The species studied are representative for the vegetation in the study area and differed significantly in chemical qualities of their litter. No significant relationships were found between decomposition rate （percentage dry mass remaining and decomposition constant k） and initial element cuncentrations.However, there were significant correlations betweeu the percentage of dry mass remaining and the mineral element concentrations in the remaining litter for most cases. The rank of the element mobility in decomposition process was as follows： Na = K 〉 Mg ≥ Ca 〉 N ≥ Mn ≥ Zn ≥ P 〉 Cu 〉〉 Al 〉〉 Fe. Concentrations of K and Na decreased in all species as decomposition proceeded. Calcium and Mg also decreased in concentrntion but with a temporal increase in the initial phase of decomposition, while the concentrations of other elements （Zn, Cu, AL and Fei increased for all species with exception of Mn which revealed a different pattern in different species. In most species, microelements （Cu, Al, and Fe） significantly increased in absolute amounts at the end of the litterbag incubation, which could be ascribed to a lange extent to the mechanism of abiotic fixation to humic substances rather than biological immobilization.