CHROMOSOMAL DIFFERENTIATION IN CLARKIA DUDLEYANA

Snow , Richard . (U. California, Davis.) Chromosomal differentiation in Clarkia dudleyana. Amer. Jour. Bot. 47 (4) : 302—309. Illus. 1960.—Clarkia dudleyana (n=9) is a common, colonial annual of the early-summer California flora. Of 275 individuals, derived from 9 natural populations and their garden-grown representatives, 17.1% were heterozygous for reciprocal translocations. Supernumerary chromosomes were also found in about 2% of the plants examined. The translocation heterozygotes are not distributed regularly over the species range but are concentrated near the geographical center of distribution. Most of the populations contained none or only a few heterozygotes, but in one colony 69% of 42 plants sampled were heterozygous. Judging from the meiotic metaphase associations observed, at least 5 different chromosome arrangements are present at this locality. Hybrids between colonies have invariably been translocation heterozygotes, the largest association found in such hybrids being a chain of all 18 chromosomes (a potential ring of 18). No correlation is evident between geographical separation and degree of cytological differentiation. Heterozygotes with smaller rings of 4 or 6 chromosomes, whether from natural populations or resulting from interpopulation hybridization, are highly fertile owing to the regular alternate disjunction of the chromosomes of the rings. In the larger rings of 12 to 18 chromosomes, derived from interpopulation crosses, segregation is much more irregular and leads to high sterility. It is possible that at least in some localities the heterozygotes enjoy a selective advantage over their homozygous sibs. It is also postulated that homozygosity for a particular chromosome arrangement may be selectively favored in a certain habitat, as a result of a position effect attendant upon placing formerly non-linked genes in the same linkage group through reciprocal translocation. The high degree of chromosomal differentiation between some populations of this species suggests that the complex heterozygotes of Oenothera have arisen as a result of hybridization of cytologically differentiated races.     

Hypoxanthine phosphoribosyltransferase activity in tissues and hypoxanthine concentrations in plasma and CSF of the horse in comparison with other species

1. Plasma hypoxanthine and xanthine concentrations are very low in the horse and low in rat, mouse and greyhound compared to concentrations in beagles, man, sheep and rabbit. 2. Activities in erythrocytes of the main enzyme metabolizing hypoxanthine, hypoxanthine phosphori-bosyltransferase, show a similar pattern (Tax et al., 1976, Comp. Biochem. Physiol. 54B, 209-212); thus low activities have been found where plasma concentrations were low. 3. Hypoxanthine phosphoribosyltransferase activities in horse tissue other than erythrocytes are similar to those in man and rabbit with high activities in brain; this enzyme may therefore be functionally important in equine brain.     

Evolution of the 28S ribosomal RNA gene in anurans: regions of variability and their phylogenetic implications

Fifteen restriction sites were mapped to the 28S ribosomal RNA gene of individuals representing 54 species of frogs, two species of salamanders, a caecilian, and a lungfish. Eight of these sites were present in all species examined, and two were found in all but one species. Alignment of these conserved restriction sites revealed, among anuran 28S rRNA genes, five regions of major length variation that correspond to four of 12 previously identified divergent domains of this gene. One of the divergent domains (DD8) consists of two regions of length variation separated by a short segment that is conserved at least throughout tetrapods. Most of the insertions, deletions, and restriction-site variations identified in the 28S gene will require sequence-level analysis for a detailed reconstruction of their history. However, an insertion in DD9 that is coextensive with frogs in the suborder Neobatrachia, a BstEII site that is limited to representatives of two leptodactylid subfamilies, and a deletion in DD10 that is found only in three ranoid genera are probably synapomorphies.      

Drosophila neuroglian: a member of the immunoglobulin superfamily with extensive homology to the vertebrate neural adhesion molecule L1

Drosophila neuroglian is an integral membrane glycoprotein that is expressed on a variety of cell types in the Drosophila embryo, including expression on a large subset of glial and neuronal cell bodies in the central and peripheral nervous systems and on the fasciculating axons that extend along them. Neuroglian cDNA clones were isolated by expression cloning. cDNA sequence analysis reveals that neuroglian is a member of the immunoglobulin superfamily. The extracellular portion of the protein consists of six immunoglobulin C2-type domains followed by five fibronectin type III domains. Neuroglian is closely related to the immunoglobulin-like vertebrate neural adhesion molecules and, among them, shows most extensive homology to mouse L1. Its homology to L1 and its embryonic localization suggest that neuroglian may play a role in neural and glial cell adhesion in the developing Drosophila embryo. We report here on the identification of a lethal mutation in the neuroglian gene.     

Characterization of cross-bridge elasticity and kinetics of cross-bridge cycling during force development in single smooth muscle cells

Force development in smooth muscle, as in skeletal muscle, is believed to reflect recruitment of force-generating myosin cross-bridges. However, little is known about the events underlying cross-bridge recruitment as the muscle cell approaches peak isometric force and then enters a period of tension maintenance. In the present studies on single smooth muscle cells isolated from the toad (Bufo marinus) stomach muscularis, active muscle stiffness, calculated from the force response to small sinusoidal length changes (0.5% cell length, 250 Hz), was utilized to estimate the relative number of attached cross-bridges. By comparing stiffness during initial force development to stiffness during force redevelopment immediately after a quick release imposed at peak force, we propose that the instantaneous active stiffness of the cell reflects both a linearly elastic cross-bridge element having 1.5 times the compliance of the cross-bridge in frog skeletal muscle and a series elastic component having an exponential length-force relationship. At the onset of force development, the ratio of stiffness to force was 2.5 times greater than at peak isometric force. These data suggest that, upon activation, cross-bridges attach in at least two states (i.e., low-force-producing and high-force-producing) and redistribute to a steady state distribution at peak isometric force. The possibility that the cross-bridge cycling rate was modulated with time was also investigated by analyzing the time course of tension recovery to small, rapid step length changes (0.5% cell length in 2.5 ms) imposed during initial force development, at peak force, and after 15 s of tension maintenance. The rate of tension recovery slowed continuously throughout force development following activation and slowed further as force was maintained. Our results suggest that the kinetics of force production in smooth muscle may involve a redistribution of cross-bridge populations between two attached states and that the average cycling rate of these cross-bridges becomes slower with time during contraction.     

Evaluation of a system for the imposition of plant water stress

A system which imposes a range of water stress levels was developed and evaluated. Water stress was controlled by employing a screen to suspend roots above a water column of known height. Levels of water stress were imposed by changing water column height and/or hydraulic conductivity of the medium in the column. The system was evaluated in a series of growth chamber experiments in which sunflowers (Helianthus annuus L. cv NK894) were given three levels of water availability for a period of 3 weeks. Third leaf midday water potentials at the end of the trials ranged from −0.73 ± 0.04 to −2.35 ± 0.17 megapascals in waterstressed plants compared to −0.40 ± 0.02 megapascals for control plants. Repetition of experiments showed no statistical differences in leaf water potentials, plant leaf areas, or plastochron indices between trials. During the experiments, the severity and pattern of water stress developments was related to both water column height and conductivity of the medium. Control plants exhibited normal diurnal water relations and transpirational behavior. Use of this system avoids many problems associated with other techniques and provides a means for subjecting plants to reproducible water stress levels for extended periods of time.     

The inheritance of skeletal muscle fibre composition in mice

Two inbred strains of mice C3H/HE and SWR, and generations produced by intercrossing, were studied to investigate the effect of heredity on muscle composition. The data were found to be consistent with a polygenic mode of inheritance. No simple effect of sex-linkage or maternal influence was evident. The heritability of fibre type percentage total fibre number and the relative size of Type I and Type II fibres were highly significant. Principal component analysis yielded a "genetic" vector which accounted for 57% of the variation in muscle fibre composition. Patterns of covariance of fibre type percentage, total fibre number and relative sizes of Type I and Type II fibres showed a single correlated response.     

Metabolic response of equine muscle to intermittent maximal exercise

Four thoroughbred horses performed 4 gallops (G1-G4) with intervals of 5 min. With one exception, gallops were sustained at maximal speed over 620 m. Muscle biopsy samples of the middle gluteal and brachiocephalicus were taken before, during, and after exercise and assayed for ATP and intermediary metabolites. The results showed a major involvement of the brachiocephalicus, in addition to the middle gluteal, during galloping. In three horses, who were clearly fatigued, muscle ATP decreased by up to 50% by the end of G4. This was matched by an equal rise in inosine 5'-monophosphate. Pronounced accumulations of glycerol 3-phosphate, glycerol, and lactate (up to 204 mmol X kg dry muscle-1) occurred with exercise. In the fourth horse, which was less fatigued, a decrease in ATP and increases in intermediary metabolites were much less. Postexercise there was little or no recovery in muscle ATP or lactate during 30 min. The decreases in ATP are consistent with a high activity of adenosine 5'-monophosphate deaminase in horse muscle and indicative also of the high level of anaerobic stress of the exercise program. There was evidence to suggest that the increase in muscle glycerol resulted from hydrolysis of glycerol 3-phosphate and not from the utilization of triglyceride.