Structure of a genomic clone encoding biologically active human relaxin

Relaxin is a peptide hormone synthesized in the corpora lutea of ovaries during pregnancy and is released into the blood stream prior to parturition. Its major biological effect is to remodel the mammalian reproductive tract to facilitate the birth process. Determination of the structure of human relaxin is thus a first step in opening up the possibility of clinical intervention in cases of difficult labour. However, the limited availability of human ovaries during pregnancy has prevented both direct amino acid sequence determination and isolation of cDNA clones obtained from relaxin producing tissue. Our approach has therefore been to screen directly for a human relaxin gene using an homologous porcine relaxin cDNA probe. We report here the successful identification of a genomic clone from which the structure of the entire coding region of a human preprorelaxin gene has been determined. Synthesis of biologically active relaxin has shown that the novel gene structure described herein codes for an authentic human relaxin. We believe this is the first successful synthesis of a biologically active hormone whose structure was predicted solely from the structure of a genomic clone.     

Brain concentrations of LSD-25 (delysid) after intracerebral or intravenous administration in conscious animals

Zusammenfassung Die Radioaktivität in Gehirn, Leber und Dünndarm der Maus nach intravenöser und nach intrazerebraler Injektion von¹⁴C-Lysergsäure-diäthylamid (Delysid) wurde bestimmt. Es ergibt sich, dass die radioaktive Substanz nach intrazerebraler Injektion mindestens ebenso schnell in der Leber erscheint und durch die Galle in den Dünndarm ausgeschieden wird, als das bei intravenöser Anwendung der Fall ist. Da nach intravenöser Injektion des markierten Delysids nur eine minimale Aktivität im Gehirn erreicht wird, kann geschlossen werden, dass die Blut-Liquor-Schranke wohl den Übertritt des Delysides vom Blut ins Gehirn weitgehend hemmt, aber den Austritt der Verbindung aus dem Gehirn nicht behindert.Die schnelle Ausscheidung von¹⁴C-markiertem Delysid aus dem Gehirn nach intraventrikulärer Injektion wurde in Versuchen an der Katze bestätigt.     

FAS and NF-κB signalling modulate dependence of lung cancers on mutant EGFR

Human lung adenocarcinomas with activating mutations in EGFR (epidermal growth factor receptor) often respond to treatment with EGFR tyrosine kinase inhibitors (TKIs), but the magnitude of tumour regression is variable and transient. This heterogeneity in treatment response could result from genetic modifiers that regulate the degree to which tumour cells are dependent on mutant EGFR. Through a pooled RNA interference screen, we show that knockdown of FAS and several components of the NF-κB pathway specifically enhanced cell death induced by the EGFR TKI erlotinib in EGFR-mutant lung cancer cells. Activation of NF-κB through overexpression of c-FLIP or IKK (also known as CFLAR and IKBKB, respectively), or silencing of IκB (also known as NFKBIA), rescued EGFR-mutant lung cancer cells from EGFR TKI treatment. Genetic or pharmacologic inhibition of NF-κB enhanced erlotinib-induced apoptosis in erlotinib-sensitive and erlotinib-resistant EGFR-mutant lung cancer models. Increased expression of the NF-κB inhibitor IκB predicted for improved response and survival in EGFR-mutant lung cancer patients treated with EGFR TKI. These data identify NF-κB as a potential companion drug target, together with EGFR, in EGFR-mutant lung cancers and provide insight into the mechanisms by which tumour cells escape from oncogene dependence.     

Correlation between acidic phospholipids and serotonin and between lysolecithin and dopamine in ganglia of the marine mussel,Mytilus edulis

Summary These studies have demonstrated a positive correlation between the acidic phospholipids and the serotonin content and between the lysolecithin and the dopamine content in the cerebral, pedal and visceral ganglia ofMytilus edulis. These relationships were further supported by experiments utilizing 6-hydroxydopamine and 5,6-dihydroxytryptamine.This study was partially supported by USPHS grant NS 10845 to Dr E. Aiello of Fordham University.Presently at Medgar Evers College of C.U.N.Y., Brooklyn, N.Y. 11225.     

Integrating genomics against infectious disease

The most recent National Academies Keck Futures Initiative Conference, entitled 'The Genomics Revolution: Implications for Treatment and Control of Infectious Disease', was held at the Arnold and Mabel Beckman Center in Irvine, California. It provided strategies and opportunities for interdisciplinary collaboration and incentives to innovate.     

热处理作用下碳钢氢腐蚀裂纹愈合规律

对含氢腐蚀裂纹的碳钢进行再热处理后,SEM观察表明,氢蚀裂发生了不同程度的愈合,实验结果表明：长度约为10μm的碳钢氢蚀裂纹完全愈合的热处理条件下是从室温到1000℃热循环5次,共10h,氢蚀裂纹的愈合机制是热扩散,发生氢蚀裂纹愈合的动力是氢蚀气泡或裂纹长大导致的塑性变 能E8。在铁、碳和氢原子扩散都足够快的情况下,氢蚀裂纹愈合的条件是E8大于裂纹愈合所必须克服的表面张力能。