First identification of a trail pheromone of an army ant (Aenictus species)

Totally blind army ants carry out massive and highly organised foraging raids, apparently guided by chemical stimuli. Until now, this phenomenon has not been closely analysed. The existence of a trail pheromone in a postpygidial gland of anAenictus species has been demonstrated and the substances identified as methyl anthranilate and methyl nicotinate The pheromone consists of two parts: a primer effect, caused by methyl nicotinate, which prepares workers to follow trails, but is not itself followed, and a releaser effect, due to methyl anthranilate, which causes trail-following only in conjunction with the primer substance.     

机械球磨方法合成稀土过渡族氧化物

采用机械球磨的方法，为合成稀土过渡族氧化物的固溶体La1-xEuxFeO3提供了新的方法和手段。对球磨合成的样品进行x—ray衍射分析。结果表明：随着球磨时间的增加，合成的效果变好，衍射峰的强度下降，衍射峰越来越宽，粒度越来越小。     

Bcr encodes a GTPase-activating protein for p21rac

More than thirty small guanine nucleotide-binding proteins related to the ras-encoded oncoprotein, termed Ras or p21ras, are known. They regulate many fundamental processes in all eukaryotic cells, such as growth, vesicle traffic and cytoskeletal organization. GTPase-activating proteins (GAPs) accelerate the intrinsic rate of GTP hydrolysis of Ras-related proteins, leading to down-regulation of the active GTP-bound form. For p21ras, two GAP proteins are known, rasGAP and the neurofibromatosis (NF1) gene product. There is evidence that rasGAP may also be a target protein for regulation by Ras and be involved in downstream signalling. We have purified a GAP protein for p21rho, which is involved in the regulation of the actin cytoskeleton. Partial sequencing of rhoGAP reveals significant homology with the product of the bcr (breakpoint cluster region) gene, the translocation breakpoint in Philadelphia chromosome-positive chronic myeloid leukaemias. We show here that the carboxy-terminal domains of the bcr-encoded protein (Bcr) and of a Bcr-related protein, n-chimaerin, are both GAP proteins for the Ras-related GTP-binding protein, p21rac. This result suggest that Bcr could be a target for regulation by Rac and has important new implications for the role of bcr translocations in leukaemia.