Desempenho agronomico e caracteristicas da cultivar de trigo BRS 49 no Estado do Parana.

A cultivar de trigo BRS 49, desenvolvida pela Embrapa Trigo, foi indicada para semeadura no Estado do Parana, a partir de 1999. Para a determinacao do seu valor de cultivo e uso, foram utilizados dados de 54 experimentos, instalados em nove locais das regioes 6, 7 e 8 do Parana, no periodo de 1996 a 1998. Apresenta como principais caracteristicas: ciclo intermediario, altura media a alta, moderada resistencia ao acamamento, tolerancia ao aluminio toxico no solo, moderada resistencia ao oidio (Blumeria graminis f. sp tritici) e a ferrugem da folha (Puccinia recondita f. sp. tritici), com percentuais de severidade em ensaios inferiores aos das testemunhas Trigo BR 23 e Trigo BR 35, suscetibilidade a giberela (Giberella zeae), cujas notas foram superiores as atribuidas as testemunhas, elevado potencial de rendimento e boa qualidade industrial. No trienio considerado, apresentou rendimento medio de 4.667 kg/ha na Regiao 6, 3.432 kg/ha, na Regiao 7, e 3.930 kg/ha, na regiao 8. Esses valores foram 11%, 11% e 28%, respectivamente, superiores a media das testemunhas (Trigo BR 2, Trigo BR 35 e CEP 24-Industrial). Os percentuais de resposta ao controle fitossanitario foram, em geral, inferiores aos observados nas referidas testemunhas, evidenciando o elevado potencial de rendimento da cultivar com aplicacoes reduzidas de fungicidas. A forca geral de gluten (W), na media de 14 amostras coletadas nas tres Regioes, foi de 260 e a relacao P/L foi de 0,685. Portanto, a cultivar se enquadra na classe Trigo Pao, de acordo com a Instrucao Normativa n.1, de 27 de janeiro de 1999 do MA. A cultivar apresenta caracteristicas de interesse agronomico, principalmente por possibilitar a obtencao de altos rendimentos, sem a necessidade de elevados investimentos com fungicidas.

Practice Links [Issue 49, October, 2012]

Practice Links is a free e-publication for practitioners working in Irish social services, voluntary and nongovernmental sectors. Practice Links was created to enable practitioners to keep up-to-date with new publications, electronic resources and conference opportunities. Issue 49 contains information regarding dance therapy for schizophrenia and the role mindfulness based stress reduction (MBSR) plays in improving the lives of adults. The issue also contains details of employment opportunities in Australia.

Yeast screens identify the RNA polymerase II CTD and SPT5 as relevant targets of BRCA1 interaction.

BRCA1 has been implicated in numerous DNA repair pathways that maintain genome integrity, however the function responsible for its tumor suppressor activity in breast cancer remains obscure. To identify the most highly conserved of the many BRCA1 functions, we screened the evolutionarily distant eukaryote Saccharomyces cerevisiae for mutants that suppressed the G1 checkpoint arrest and lethality induced following heterologous BRCA1 expression. A genome-wide screen in the diploid deletion collection combined with a screen of ionizing radiation sensitive gene deletions identified mutants that permit growth in the presence of BRCA1. These genes delineate a metabolic mRNA pathway that temporally links transcription elongation (SPT4, SPT5, CTK1, DEF1) to nucleopore-mediated mRNA export (ASM4, MLP1, MLP2, NUP2, NUP53, NUP120, NUP133, NUP170, NUP188, POM34) and cytoplasmic mRNA decay at P-bodies (CCR4, DHH1). Strikingly, BRCA1 interacted with the phosphorylated RNA polymerase II (RNAPII) carboxy terminal domain (P-CTD), phosphorylated in the pattern specified by the CTDK-I kinase, to induce DEF1-dependent cleavage and accumulation of a RNAPII fragment containing the P-CTD. Significantly, breast cancer associated BRCT domain defects in BRCA1 that suppressed P-CTD cleavage and lethality in yeast also suppressed the physical interaction of BRCA1 with human SPT5 in breast epithelial cells, thus confirming SPT5 as a relevant target of BRCA1 interaction. Furthermore, enhanced P-CTD cleavage was observed in both yeast and human breast cells following UV-irradiation indicating a conserved eukaryotic damage response. Moreover, P-CTD cleavage in breast epithelial cells was BRCA1-dependent since damage-induced P-CTD cleavage was only observed in the mutant BRCA1 cell line HCC1937 following ectopic expression of wild type BRCA1. Finally, BRCA1, SPT5 and hyperphosphorylated RPB1 form a complex that was rapidly degraded following MMS treatment in wild type but not BRCA1 mutant breast cells. These results extend the mechanistic links between BRCA1 and transcriptional consequences in response to DNA damage and suggest an important role for RNAPII P-CTD cleavage in BRCA1-mediated cancer suppression.