The synaptic origins of receptive field properties in the cricket cercal sensory system

Summary The regional distribution of cerebral glucose utilization, revealed by the¹⁴C-2DG technique, was compared between (i) toads after stimulus-specific long-term habituation of the orienting response toward a repeatedly presented prey dummy (habituation group) and (ii) non-habituated toads, readily orienting toward the repetitively presented prey stimulus (naive group). In the habituation group, the ventral medial pallium (vMP), a certain portion of the preoptic area (PO), and the dorsal hypothalamus (dHYP) showed a statistically significantincrease in¹⁴C-2DG-uptake;decrease was observed in the ventral layers of the optic tectum (vOT), a portion of the tegmental reticular formation (RET), the ventral cerebellum (vCB), and the striatum (STR). The results suggest that stimulus-specific long-term habituation of prey-catching affects both, components of thestimulus-response mediating circuit (e.g., involving OT), and structures extrinsic to it, (e.g., vMP, PO, dHYP), which may belong to amodulatory circuitry. Bilateral lesions to vMP strongly delay habituation. Our results are suggesting that damping of the adequate behavioral motor response during habituation involves active inhibitory processes of a modulatory system that develops in strength during stimulus repetition so as to suppress response output, which basically supports Sokolov's hypothesis (1975).Abbreviations A anterior dorsal thalamic nucleus - AL amygdala, lateral portion - dCB dorsal half of the cerebellum - vCB ventral half of the cerebellum - DP dorsal pallium - dHYP dorsal hypothalamus - pLP posterior half of the lateral pallium - Lpd lateral postero-dorsal thalamus - Lpv lateral postero-ventral thalamus - aMP anterior third of the medial pallium - dMP dorsal portion of the posterior medial pallium - vMP ventral two-third of the posterior medial pallium - MS medial septum - dOT dorsal layers of the optic tectum - vOT ventral layers of the optic tectum - P posterior thalamic nucleus - PO preoptic area - RET tegmental portion of the medial reticular formation - STR striatum, dorsal and ventral portion - vTEG ventral tegmentum     

The refinement of invertebrate synapses during development

Evidence is provided that during invertebrate development synapses undergo a period of refinement during which there are changes in synaptic connectivity and specific synaptic properties. It appears that extrinsic cues such as competition and neural activity are involved in guiding these synaptic changes in invertebrates. Comparisons are made with findings in the vertebrate literature.     

Diversity among bacteria isolated from the deep subsurface

Culturable bacteria from the deep subsurface (179 m) at Cerro Negro, New Mexico were isolated and characterized. The average number of viable aerobic bacteria was estimated to be 5×10⁵g^–1 of sediment, but only about 0.1% of these could be recovered on agar medium when incubated under aerobic conditions. Of 158 strains isolated from this depth, 92 were characterized by cellular fatty acid profiles (FAME), 36 by analysis of partial 16S rDNA sequences, and 44 by rep-PCR genome fingerprint analysis using three different sets of oligonucleotide primers (REP, BOX, or ERIC). These analyses showed the majority of isolates (67%) were Gram-positive bacteria and primarily members of genera with a high %G+C DNA. The remaining isolates were -subdivisionProteobacteria (19%) and members of the flavobacteria group (14%). The diversity indices based on these different methods of characterization were very high suggesting this subsurface habitat harbors a highly diverse microbial community.     

Genetic control of sexually dimorphic axon morphology in Drosophila sensory neurons

The mechanism by which orderly axonal projections are formed during development remains an important and largely unsolved problem in neurobiology. It may be possible to examine the control of axon growth in Drosophila and take advantage of genetic tools to better understand the phenomenon. We show here that some gustatory axons in Drosophila are sexually dimorphic and that genes involved in sex determination control the anatomy of these axons. Both males and females possess gustatory receptors on their legs but males possess more of these receptors than females. More significantly, the axons of the male receptors usually cross the midline and they never do so in females, indicating a central zone of bilateral input in the male but not in the female nervous system. In chromosomal females, expressing a tra or Sxl mutation, the gustatory system is transformed toward the male phenotype. Mutant XX adults resemble normal males externally, because they have more gustatory receptors, and internally, because their axons cross the midline. Gynandromorphs show that the sex of the sensory neuron, and apparently not the central nervous system, controls the growth of the axons. We conclude that the anatomical site of control for this dimorphism is the gustatory neurons.     

Impaired myogenic constriction of the renal afferent arteriole in a mouse model of reduced βENaC expression

Previous studies demonstrate a role for β epithelial Na(+) channel (βENaC) protein as a mediator of myogenic constriction in renal interlobar arteries. However, the importance of βENaC as a mediator of myogenic constriction in renal afferent arterioles, the primary site of development of renal vascular resistance, has not been determined. We colocalized βENaC with smooth muscle α-actin in vascular smooth muscle cells in renal arterioles using immunofluorescence. To determine the importance of βENaC in myogenic constriction in renal afferent arterioles, we used a mouse model of reduced βENaC (βENaC m/m) and examined pressure-induced constrictor responses in the isolated afferent arteriole-attached glomerulus preparation. We found that, in response to a step increase in perfusion pressure from 60 to 120 mmHg, the myogenic tone increased from 4.5 ± 3.7 to 27.3 ± 5.2% in +/+ mice. In contrast, myogenic tone failed to increase with the pressure step in m/m mice (3.9 ± 0.8 to 6.9 ± 1.4%). To determine the importance of βENaC in myogenic renal blood flow (RBF) regulation, we examined the rate of change in renal vascular resistance following a step increase in perfusion pressure in volume-expanded animals. We found that, following a step increase in pressure, the rate of myogenic correction of RBF is inhibited by 75% in βENaC m/m mice. These findings demonstrate that myogenic constriction in afferent arterioles is dependent on normal expression of βENaC.     

Retrograde signaling and the development of transmitter release properties in the invertebrate nervous system

The dynamics of presynaptic transmitter release are oftern matched to the functional properties of the prostsynaptic cell. In organisms ranging from cats to crickets, evidence suggests that retrograde signaling is essential for matching these presynaptic release properties to individual postsynaptic partners. Retrograde interactions appear to control the development of presynaptic, short-term facilitation and depression. 1994 John Wiley & Sons, Inc.     

广义隐Markov模型在基因识别中的应用

广义隐Markov模型(GHMM)是基因识别的一种重要模型,但是其计算量比传统的隐Markov模型大得多,以至于不能直 接在基因识别中使用。根据原核生物基因的结构特点,提出了一种高效的简化算法,其计算量是序列长度的线性函数。在此 基础上,构建了针对原核生物基因的识别程序GeneMiner,对实际数据的测试表明,此算法是有效的。     

Confirmation of quantitative trait loci affecting fatness in chickens

In this report we describe the analysis of an advanced intercross line (AIL) to confirm the quantitative trait locus (QTL) regions found for fatness traits in a previous study. QTL analysis was performed on chromosomes 1, 3, 4, 15, 18, and 27. The AIL was created by random intercrossing in each generation from generation 2 (G₂) onwards until generation 9 (G₉) was reached. QTL for abdominal fat weight (AFW) and/or percentage abdominal fat (AF%) on chromosomes 1, 3 and 27 were confirmed in the G₉ population. In addition, evidence for QTL for body weight at the age of 5 (BW5) and 7 (BW7) weeks and for the percentage of intramuscular fat (IF%) were found on chromosomes 1, 3, 15, and 27. Significant evidence for QTL was detected on chromosome 1 for BW5 and BW7. Suggestive evidence was found on chromosome 1 for AFW, AF% and IF%, on chromosome 15 for BW5, and on chromosome 27 for AF% and IF%. Furthermore, evidence on the chromosome-wise level was found on chromosome 3 for AFW, AF%, and BW7 and on chromosome 27 for BW5. For chromosomes 4 and 18, test statistics did not exceed the significance threshold.