Effects of low-temperature oxidation on natural remanent magnetization of Chinese loess

This study systematically investigates changes in both compositions and grain-sizes of magnetic minerals in the Chinese loess/paleosol samples (Yichuan, China) during thermal demagnetization processes. Between 100 and 200℃, (1) H_c and H_cr significantly decrease while M_rs and M_s remain stable; (2) concentration of the multi-domain (MD) grains increases while that of superparamagnetic (SP) grains decreases; and (3) there exists the abnormal behavior of the thermal demagnetization in the natural remanent magnetization (NRM). In addition, the corresponding changes in all these parameters are gradually muted with the increase of the pedogenesis degree. The results indicate that the observed alteration probably relates to reducing processes caused by the burning of the organic matter in samples. Before the thermal treatment, the MD grains in loess samples had been partially altered in nature by low-temperature oxidization (LTO). This CRM can be sufficiently attenuated or even removed by the reducing process between 100 and 200℃ during the thermal treatment and has no apparent harmful effects on the characteristic remanent magnetization (ChRM) between 300 and 500℃.     

Induction of autophagy and inhibition of tumorigenesis by beclin 1

The process of autophagy, or bulk degradation of cellular proteins through an autophagosomic-lysosomal pathway, is important in normal growth control and may be defective in tumour cells. However, little is known about the genetic mediators of autophagy in mammalian cells or their role in tumour development. The mammalian gene encoding Beclin 1, a novel Bcl-2-interacting, coiled-coil protein, has structural similarity to the yeast autophagy gene, apg6/vps30, and is mono-allelically deleted in 40-75% of sporadic human breast cancers and ovarian cancers. Here we show, using gene-transfer techniques, that beclin 1 promotes autophagy in autophagy-defective yeast with a targeted disruption of agp6/vps30, and in human MCF7 breast carcinoma cells. The autophagy-promoting activity of beclin 1 in MCF7 cells is associated with inhibition of MCF7 cellular proliferation, in vitro clonigenicity and tumorigenesis in nude mice. Furthermore, endogenous Beclin 1 protein expression is frequently low in human breast epithelial carcinoma cell lines and tissue, but is expressed ubiquitously at high levels in normal breast epithelia. Thus, beclin 1 is a mammalian autophagy gene that can inhibit tumorigenesis and is expressed at decreased levels in human breast carcinoma. These findings suggest that decreased expression of autophagy proteins may contribute to the development or progression of breast and other human malignancies.     

Clathrin light chains contain brain-specific insertion sequences and a region of homology with intermediate filaments

The primary structures of four bovine clathrin light chains have been determined. Light chains LCa and LCb are homologous proteins encoded by different genes. In the brain the messenger RNA from these genes undergoes differential splicing to yield proteins having centrally inserted brain-specific sequences. A potentially alpha-helical region of the clathrin light chains shows homology with intermediate filament proteins.     

Chromosome morphology of sceloporine lizards (Sceloporus occidentalis andS. graciosus)

Résumé Les chromosomes somatiques de deux Lézards représentatifs des sceloporins sont analysés.S. graciosus a 12 macrochromosomes et 18 microchromosomes, etS. occidentalis a 12 macrochromosomes et 10 microchromosomes. La morphologie des macrochromosomes de ces deux espèces est la même. La morphologie des microchromosomes offre des différences spécifiques importantes. Ce fait ainsi que d'autres constatations suggèrent que les changements observés dans les microchromosomes jouent probablement un rôle important dans l'évolution du karyotype des Lézards.     

The European dimension for the mouse genome mutagenesis program

The European Mouse Mutagenesis Consortium is the European initiative contributing to the international effort on functional annotation of the mouse genome. Its objectives are to establish and integrate mutagenesis platforms, gene expression resources, phenotyping units, storage and distribution centers and bioinformatics resources. The combined efforts will accelerate our understanding of gene function and of human health and disease.