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1.
Mol Cell Biol ; 20(8): 2760-73, 2000 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-10733579

RESUMO

Ornithine decarboxylase (ODC) of the fungus Neurospora crassa, encoded by the spe-1 gene, catalyzes an initial and rate-limiting step in polyamine biosynthesis and is highly regulated by polyamines. In N. crassa, polyamines repress the synthesis and increase the degradation of ODC protein. Changes in the rate of ODC synthesis correlate with similar changes in the abundance of spe-1 mRNA. We identify two sequence elements, one in each of the 5' and 3' regions of the spe-1 gene of N. crassa, required for this polyamine-mediated regulation. A 5' polyamine-responsive region (5' PRR) comprises DNA sequences both in the upstream untranscribed region and in the long 5' untranslated region (5'-UTR) of the gene. The 5' PRR is sufficient to confer polyamine regulation to a downstream, heterologous coding region. Use of the beta-tubulin promoter to drive the expression of various portions of the spe-1 transcribed region revealed a 3' polyamine-responsive region (3' PRR) downstream of the coding region. Neither changes in cellular polyamine status nor deletion of sequences in the 5'-UTR alters the half-life of spe-1 mRNA. Sequences in the spe-1 5'-UTR also impede the translation of a heterologous coding region, and polyamine starvation partially relieves this impediment. The results show that N. crassa uses a unique combination of polyamine-mediated transcriptional and translational control mechanisms to regulate ODC synthesis.


Assuntos
Neurospora crassa/enzimologia , Ornitina Descarboxilase/biossíntese , Regiões 5' não Traduzidas , Regulação Enzimológica da Expressão Gênica , Regulação Fúngica da Expressão Gênica , Neurospora crassa/genética , Ornitina Descarboxilase/genética , Poliaminas , Transcrição Gênica
2.
Genetika ; 29(10): 1620-9, 1993 Oct.
Artigo em Russo | MEDLINE | ID: mdl-8307353

RESUMO

Chlorophyll--binding protein CP43 and cytochrome b559, encoded by psbC and psbE/F genes, are the components of photosystem II (PS II). Three psbC- and four psbE/F- mutants were isolated from the collection of PS II-deficient mutants of the cyanobacterium Synechocystis sp. 6803. Restoration of photosynthetic activity was achieved by transformation of psbE/F- mutants with cloned psbE/F gene cluster from wild type cells and each of psbC- mutants--with specific part of wild type psbC gene. DNA fragments carrying the mutations were isolated from mutant cells and sequenced. The mutations which affect PS II activity were identified in psbC gene as "frameshift" mutation, stop-codon formation, or as deletion of three nucleotides resulting in loss of one of three Phe residues in position 422-424 of CP43. Sequence of mutant psbE/F genes revealed single mutations resulting in deletion of Phe-36 or substitution of Pro-63 for Leu in alpha-subunit and Val-29 for Phe in beta-subunit of cytochrome b559.


Assuntos
Proteínas de Bactérias/genética , Cianobactérias/genética , Genes Bacterianos , Código Genético , Mutação , Complexo de Proteínas do Centro de Reação Fotossintética/genética , Complexo de Proteína do Fotossistema II , Sequência de Aminoácidos , Sequência de Bases , Grupo dos Citocromos b/genética , Dados de Sequência Molecular , Estrutura Secundária de Proteína
3.
Nurs Stand ; 8(4): 42-3, 1993 Oct 13.
Artigo em Inglês | MEDLINE | ID: mdl-27526913

RESUMO

I would like to congratulate Brennan and Williams on their thought-provoking article, Preceptorship: Is it a workable concept? (Clinical, September 15).

5.
Development ; 126(23): 5245-54, 1999 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-10556050

RESUMO

We have isolated Cngsc, a hydra homologue of goosecoid gene. The homeodomain of Cngsc is identical to the vertebrate (65-72%) and Drosophila (70%) orthologues. When injected into the ventral side of an early Xenopus embryo, Cngsc induces a partial secondary axis. During head formation, Cngsc expression appears prior to, and directly above, the zone where the tentacles will emerge, but is not observed nearby when the single apical tentacle is formed. This observation indicates that the expression of the gene is not necessary for the formation of a tentacle per se. Rather, it may be involved in defining the border between the hypostome and the tentacle zone. When Cngsc(+) tip of an early bud is grafted into the body column, it induces a secondary axis, while the adjacent Cngsc(-) region has much weaker inductive capacities. Thus, Cngsc is expressed in a tissue that acts as an organizer. Cngsc is also expressed in the sensory neurons of the tip of the hypostome and in the epithelial endodermal cells of the upper part of the body column. The plausible roles of Cngsc in organizer function, head formation and anterior neuron differentiation are similar to roles goosecoid plays in vertebrates and Drosophila. It suggests widespread evolutionary conservation of the function of the gene.


Assuntos
Padronização Corporal/genética , Proteínas Fetais , Cabeça/fisiologia , Proteínas de Homeodomínio/genética , Hydra/genética , Organizadores Embrionários/fisiologia , Proteínas Repressoras , Fatores de Transcrição , Sequência de Aminoácidos , Animais , Clonagem Molecular , Sequência Conservada , Embrião não Mamífero , Evolução Molecular , Extremidades/fisiologia , Feminino , Regulação da Expressão Gênica no Desenvolvimento , Proteína Goosecoid , Cabeça/crescimento & desenvolvimento , Proteínas de Homeodomínio/metabolismo , Hydra/embriologia , Hydra/crescimento & desenvolvimento , Dados de Sequência Molecular , Regeneração , Reprodução/genética , Homologia de Sequência de Aminoácidos , Proteínas com Domínio T/genética , Xenopus/embriologia , Xenopus/genética
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