Genetic homogeneity between acute and chronic forms of spinal muscular atrophy

The childhood-onset spinal muscular atrophies (SMAs) describe a heterogeneous group of disorders that selectively affect the alpha motoneuron. We have shown that chronic childhood-onset SMA (SMA II and III) maps to a single locus on chromosome 5q. Acute SMA (SMA Type I/Werdnig-Hoffmann/severe/infantile) is the main cause of heritable infant mortality. Mapping the acute SMA locus by conventional methods is complicated by the rapidly fatal course of the disease and its recessive mode of inheritance. We present here the typing of four inbred acute-SMA families with DNA markers on chromosome 5q and analysis of these together with acute families from our previous study to demonstrate genetic homogeneity between the acute and chronic forms of SMA. The data indicate that the acute SMA locus maps to chromosome 5q11.2-13.3. Two families seem unlinked to 5q markers, raising the possibility of genetic heterogeneity or disease misclassification within the acute and chronic family sets.     

Preliminary indications for the presence of a hypothalamic follicle stimulating hormone synthesizing factor

Résumé Après une période de 45 min, une seule injection intrajugulaire des extraits hypothalamiques provoque une chute maximale du niveau de FSH hypophysaire, qui atteste la présence de FSH-RF. Quand une seconde injection des extraits est administrée 45 min plus tard, la FSH hypophysaire est rétablie à une vitesse supérieure à celle observée chez les animaux qui n'ont reçu qu'une seule injection. Les résultats indiquent la présence possible d'un «FSH-Synthesizing Factor» (FSH-SF).     

Intercellular bridges of chick blastoderm studied by scanning and transmission electron microscopy.

Chick blastoderms were studied by scanning and transmission electron microscopy to identify by both methods a type of thread-like structure lying on the epiblast. The structure was identified by transmission microscopy as a long telophase bridge containing mid-body and spindle remnant. It appears to provide cytoplasmic continuity between only 2 cells.     

Native plants dominate understory vegetation following ponderosa pine forest restoration treatments

Dense ponderosa pine forests in the southwestern United States inhibit understory production and diversity and are susceptible to high-severity wildfire. Restoration treatments involving overstory thinning and prescribed burning are being implemented to increase understory productivity and diversity and to reduce the risk of severe wildfire. However, disturbances associated with treatments may favor invasion of nonnative species, and the severity of the disturbance may be related to the level of nonnative species establishment. We examined understory community composition, species richness, and plant cover responses to 3 stand-scale replicates of 4 different tree-thinning intensities. Restoration treatments altered the composition of the understory community regardless of thinning intensity. Understory richness and cover were highly variable among experimental blocks, but we observed strong trends of increasing richness and cover in the treated stands. Immediately following restoration treatments, nonnative species cover comprised 6% of the total cover where treatment-induced disturbances were the greatest. However, the initial increase in nonnative species did not persist and was reduced by half 6 years after treatment. Plant community composition was still in flux by the sixth year after treatment, indicating that continued monitoring is necessary for evaluating whether restoration targets are maintained over time. Los densos bosques de pino ponderosa en el suroeste de los E.U.A. inhiben la producción y diversidad del sotobosque y son propensos a incendios severos. El raleo del dosel y la quema controlada se están implementando como tratamientos de restauración para incrementar la productividad y diversidad del sotobosque y para reducir el peligro de incendios severos. Sin embargo, las perturbaciones asociadas con estos tratamientos podrían favorecer la invasión por especies no nativas, y la severidad de la perturbación puede estar relacionada con el nivel de establecimiento de estas especies. Examinamos la reacción del sotobosque con respecto a la composición de sus comunidades, a la riqueza de especies y a la cobertura de la vegetación, a tres réplicas a nivel de rodal de cuatro distintas intensidades de raleo. Los tratamientos de restauración cambiaron la composición de la comunidad del sotobosque independientemente de la intensidad del raleo. La riqueza y la cobertura del sotobosque variaron mucho entre las áreas estudiadas, pero observamos marcadas tendencias de mayor riqueza y cobertura en los rodales que recibieron el tratamiento. Inmediatamente después de los tratamientos de restauración, la cobertura de especies invasoras constituía el 6% de la cobertura total donde las perturbaciones producidas por los tratamientos fueron más grandes. No obstante, el aumento inicial en la cobertura de especies invasoras no persistió, y se redujo a la mitad en un lapso de seis años después del tratamiento. La composición de las comunidades de plantas aun seguía cambiando en el sexto año después del tratamiento, lo cual indica que será preciso el monitoreo continuo para determinar si se lograron las metas de restauración.     

Single amino acid substitutions in influenza haemagglutinin change receptor binding specificity

The haemagglutinin (HA) glycoproteins of influenza virus membranes are responsible for binding viruses to cells by interacting with membrane receptor molecules which contain sialic acid (for review see ref. 1). This interaction is known to vary in detailed specificity for different influenza viruses (see, for example, refs 2-4) and we have attempted to identify the sialic acid binding site of the haemagglutinin by comparing the amino acid sequences of haemagglutinins with different binding specificities. We present here evidence that haemagglutinins which differ in recognizing either NeuAc alpha 2 leads to 3Gal- or NeuAc alpha 2 leads to 6Gal- linkages in glycoproteins also differ at amino acid 226 of HA1. This residue is located in a pocket on the distal tip of the molecule, an area previously proposed from considerations of the three-dimensional structure of the haemagglutinin to be involved in receptor binding.