Norrie disease is caused by mutations in an extracellular protein resembling C-terminal globular domain of mucins.

A candidate gene for Norrie disease, an X-linked disorder characterized by blindness, deafness and mental disturbances, was recently isolated and found to contain microdeletions in numerous patients. No strong homologies were identified. By studying the number and spacing of cysteine residues, we now detect homologies between the Norrie gene product and a C-terminal domain which is common to a group of proteins including mucins. Three newly-characterized missense mutations, replacing evolutionarily conserved cysteines or creating new cysteine codons, emphasize the functional importance of these sites. These findings and the clinical features of this disorder suggest a possible role for the Norrie gene in neuroectodermal cell-cell interaction.     

Profound block in thymocyte development in mice lacking p56lck.

The protein Lck (p56lck) has a relative molecular mass of 56,000 and belongs to the Src family of tyrosine kinases. It is expressed exclusively in lymphoid cells, predominantly in thymocytes and peripheral T cells. Lck associates specifically with the cytoplasmic domains of both CD4 and CD8 T-cell surface glycoproteins and interacts with the beta-chain of the interleukin-2 receptor, which implicates Lck activity in signal transduction during thymocyte ontogeny and activation of mature T cells. Here we generate an lck null mutation by homologous recombination in embryonic stem cells to evaluate the role of p56lck in T-cell development and activation. Lck-deficient mice show a pronounced thymic atrophy, with a dramatic reduction in the double-positive (CD4+CD8+) thymocyte population. Mature, single-positive thymocytes are not detectable in these mice and there are only very few peripheral T cells. These results illustrate the crucial role of this T-cell-specific tyrosine kinase in the thymocyte development.     

The occurrence of Δ3-trans-hexadecenoic acid in phosphatidyl glycerol from spinach leaves

Zusammenfassung Der Gehalt an ³-trans-Hexadecensäure im Phosphatidylglycerol aus grünen Spinatblättern (Spinacea oleracea) erweist sich als auffallend hoch. Die enzymatische Hydrolyse zeigt die C₁₆-Monoensäure mit der-Stelle des Phosphatids verknüpft.     

Essais d'inhibition de l'action inflammatoire cutanée du chloroforme chez le rat

Summary (1)—In the rat, total extracts of cortex, cortisone and A.C.T.H. do not retard the fixation of a vital colorant at the level of a cutaneous zone irritated by chloroform.(2)—Phenergan prolongs the delay in the appearance of the blue.(3)—Sodium salicylate selectively inhibits the inflammatory cutaneous action of chloroform, even after adrenalectomy.