The white gene of Drosophila melanogaster encodes a protein with a role in courtship behavior.

The white gene of Drosophila melanogaster has been extensively studied, yet it is still not understood how its ectopic overexpression induces male-male courtship. To investigate the cellular basis of this behavior, we examined the sexual behavior of several classes of mutants. We find that male-male courtship is seen not only in flies overexpressing the white gene, but also in mutants expected to have mislocalized White protein. This finding confirms that mislocalizing White transporter in the cells in which it is normally expressed will produce male-male courtship behaviors; the courtship behavior is not an indirect consequence of aberrant physiological changes elsewhere in the body. Male-male courtship is also seen in some mutants with altered monoamine metabolism and deficits in learning and memory, but can be distinguished from that produced by White mislocalization by its reduced intensity and locomotor activity. Double mutants overexpressing white and with mutations in genes for serotonergic neurons suggest that male-male courtship produced by mislocalizing White may not be mediated exclusively by serotonergic neurons. We also find decreased olfactory learning in white mutants and in individuals with mutations in the genes for White's binding partners, brown and scarlet. Finally, in cultured Drosophila and mammalian cells, the White transporter is found in the endosomal compartment. The additional genes identified here as being involved in male-male courtship increase the repertoire of mutations available to study sexual behavior in Drosophila.

Consistency of visual assessments of mammographic breast density from vendor-specific "for presentation" images.

Discussions of percent breast density (PD) and breast cancer risk implicitly assume that visual assessments of PD are comparable between vendors despite differences in technology and display algorithms. This study examines the extent to which visual assessments of PD differ between mammograms acquired from two vendors. Pairs of "for presentation" digital mammography images were obtained from two mammography units for 146 women who had a screening mammogram on one vendor unit followed by a diagnostic mammogram on a different vendor unit. Four radiologists independently visually assessed PD from single left mediolateral oblique view images from the two vendors. Analysis of variance, intra-class correlation coefficients (ICC), scatter plots, and Bland-Altman plots were used to evaluate PD assessments between vendors. The mean radiologist PD for each image was used as a consensus PD measure. Overall agreement of the PD assessments was excellent between the two vendors with an ICC of 0.95 (95% confidence interval: 0.93 to 0.97). Bland-Altman plots demonstrated narrow upper and lower limits of agreement between the vendors with only a small bias (2.3 percentage points). The results of this study support the assumption that visual assessment of PD is consistent across mammography vendors despite vendor-specific appearances of "for presentation" images.

Colonic nociception via nucleus submedius is modulated by pontine centres in the rat.

The rat thalamic nucleus submedius responds to noxious pressure stimuli in the colon. Some neurons in and near Barrington's nucleus, a pontine center related to bladder function, also respond to colon distension. We hypothesized that colonic nociception may be relayed via Barrington's nucleus to the nucleus submedius. Experiments were carried out in 22 urethane-anesthetized male rats. Noxious stimuli were applied to the toes using standardized clips and to the colon by inflation of the balloon to 80 mmHg for 30 s using a barostat. The brain was exposed to allow recording from the nucleus submedius with a monopolar tungsten electrode and the activity of rectus muscle was assessed via silver wire electrodes. A glass pipette was inserted into Barrington's nucleus for injection of 5 mM CoCl2, a temporary neural blocker. The site of CoCl2 injection was confirmed by the presence of FluoroGold which was incorporated into the CoCl2 solution. We recorded 51 units in submedius that were excited by noxious toe pinch, 4 were inhibited. Colon distension to 80 mmHg produced visceromotor responses, excited 23 units in submedius and inhibited 13 units. Injection of CoCl2 into the region of Barrington's nucleus blocked the response to colon distension in 10 of 12 Sm units tested, but had no influence on the accompanying visceromotor response. These data point to a previously unrecognized relationship between Barrington's nucleus and submedius that may subserve colon nociception.