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1.
Curr Genomics ; 10(8): 540-9, 2009 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-20514216

RESUMO

Natural variation provides a valuable resource to study the genetic regulation of quantitative traits. In quantitative trait locus (QTL) analyses this variation, captured in segregating mapping populations, is used to identify the genomic regions affecting these traits. The identification of the causal genes underlying QTLs is a major challenge for which the detection of gene expression differences is of major importance. By combining genetics with large scale expression profiling (i.e. genetical genomics), resulting in expression QTLs (eQTLs), great progress can be made in connecting phenotypic variation to genotypic diversity. In this review we discuss examples from human, mouse, Drosophila, yeast and plant research to illustrate the advances in genetical genomics, with a focus on understanding the regulatory mechanisms underlying natural variation. With their tolerance to inbreeding, short generation time and ease to generate large families, plants are ideal subjects to test new concepts in genetics. The comprehensive resources which are available for Arabidopsis make it a favorite model plant but genetical genomics also found its way to important crop species like rice, barley and wheat. We discuss eQTL profiling with respect to cis and trans regulation and show how combined studies with other 'omics' technologies, such as metabolomics and proteomics may further augment current information on transcriptional, translational and metabolomic signaling pathways and enable reconstruction of detailed regulatory networks. The fast developments in the 'omics' area will offer great potential for genetical genomics to elucidate the genotype-phenotype relationships for both fundamental and applied research.

2.
Int Rev Cytol ; 201: 209-75, 2001.
Artigo em Inglês | MEDLINE | ID: mdl-11057833

RESUMO

Mitogen-activated protein kinases (MAPKs) are important signaling tools in all eukaryotes, and function in mediating an enormous variety of external signals to appropriate cellular responses. MAPK pathways have been studied extensively in yeast and mammalian cells, and a large body of knowledge on their functioning has accumulated, which is summarized briefly. Plant MAPK pathways have attracted increasing interest, resulting in the isolation of a large number of different components of MAPK cascades. Studies on the functions of these components have revealed that MAPKs play important roles in the response to a broad variety of stresses, as well as in the signaling of most plant hormones and in developmental processes. Finally, the involvement of various plant phosphatases in the inactivation of MAPKs is discussed.


Assuntos
Sistema de Sinalização das MAP Quinases/fisiologia , Células Vegetais , Plantas/metabolismo , Ciclo Celular/fisiologia , Células Eucarióticas/citologia , Células Eucarióticas/metabolismo , Regulação da Expressão Gênica de Plantas/fisiologia , MAP Quinase Quinase Quinases/metabolismo , Quinases de Proteína Quinase Ativadas por Mitógeno/metabolismo , Proteínas Quinases Ativadas por Mitógeno/metabolismo , Filogenia , Doenças das Plantas/genética , Reguladores de Crescimento de Plantas/metabolismo , Estrutura Terciária de Proteína/fisiologia , Cicatrização/fisiologia
4.
J Biol Chem ; 275(47): 36734-40, 2000 Nov 24.
Artigo em Inglês | MEDLINE | ID: mdl-10973984

RESUMO

Plant cells respond to elicitors by inducing a variety of defense responses. Some of these reactions are dependent on the activity of protein kinases. Recently, mitogen-activated protein kinases (MAPKs) have been identified to be activated by fungal and bacterial elicitors as well as by pathogen infection. In gel kinase assays of alfalfa cells treated with yeast cell wall-derived elicitor (YE) revealed that 44- and 46-kDa MAPKs are rapidly and transiently activated. Immunokinase assays with specific MAPK antibodies revealed that YE mainly activated the 46-kDa SIMK and the 44-kDa MMK3 and to a lesser extent the 44-kDa MMK2 and SAMK. When cells were treated with chemically defined elicitors potentially contained in the YE (chitin and N-acetylglucosamine oligomers, beta-glucan, and ergosterol), the four MAPKs were found to be activated to different levels and with different kinetics. Whereas SIMK and SAMK have been found to be activated by a number of diverse stimuli, MMK3 is activated during mitosis and was therefore assumed to participate in cell division (). No physiological process could be associated with MMK2 activity so far. This is the first report that MMK2 and MMK3 can be activated by external stimuli. Overall, our findings indicate that plant cells can sense different cues of a given microorganism through the activation of multiple MAPKs.


Assuntos
Proteínas Quinases Ativadas por Mitógeno/metabolismo , Proteínas de Plantas , Plantas/enzimologia , beta-Glucanas , Células Cultivadas , Quitina/metabolismo , Ativação Enzimática , Ergosterol/metabolismo , Glucanos/metabolismo , Medicago sativa/enzimologia , Peso Molecular
5.
Plant Cell Physiol ; 41(6): 692-701, 2000 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-10945338

RESUMO

Cultured parsley (Petroselinum crispum) cells respond to treatment with elicitors derived from different species of the genus Phytophthora with transcript accumulation of defense-associated genes and the production of furanocoumarin phytoalexins. Pep-25, an oligopeptide fragment of a Phytophthora sojae 42-kDa cell wall protein, and a cell wall elicitor preparation derived from Phytophthora parasitica (Pp-elicitor) stimulate accumulation of the same gene transcripts and formation of the same pattern of furanocoumarins. Treatment of cultured cells and protoplasts with proteinase-digested Pp-elicitor identified proteinaceous constituents as active eliciting compounds in parsley. Similar to Pep- 25, Pp-elicitor induced effluxes of K+ and Cl- and influxes of protons and Ca2+. Concomitantly, as monitored in aequorin-transgenic parsley cell lines both elicitors induced an immediate increase in the cytoplasmic Ca2+ concentration up to sustained levels of 175 nM (Pp-elicitor) or 300 nM (Pep-25), respectively. The signature of the Ca2+ response differed greatly between the two elicitors tested. Extracellular Ca2+ proved essential for activation of an oxidative burst, MAP kinase activity and phytoalexin production by either elicitor. While Pp-elicitor induced a qualitatively similar spectrum of defense responses as did Pep-25, elicitor-specific quantitative differences in response intensity and kinetics suggest activation of a conserved signaling cascade through separate ligand binding sites.


Assuntos
Apiaceae/microbiologia , Apiaceae/fisiologia , Proteínas Fúngicas/farmacologia , Regulação da Expressão Gênica de Plantas/fisiologia , Glicoproteínas de Membrana/farmacologia , Phytophthora , Apiaceae/efeitos dos fármacos , Cálcio/metabolismo , Parede Celular/fisiologia , Células Cultivadas , Cloretos/metabolismo , Regulação da Expressão Gênica de Plantas/efeitos dos fármacos , Fragmentos de Peptídeos/farmacologia , Extratos Vegetais/genética , Potássio/metabolismo , Protoplastos/fisiologia , Sesquiterpenos , Terpenos , Fitoalexinas
6.
Results Probl Cell Differ ; 27: 11-27, 2000.
Artigo em Inglês | MEDLINE | ID: mdl-10533195

RESUMO

Mitogen-activated protein kinase (MAPK) pathways are protein kinase cascades that have a function in the transduction of extracellular signals to intracellular targets in all eukaryotes. Distinct MAPK pathways are regulated by different signals and have a role in a wide variety of physiological processes. In plants there is evidence for a role of MAPKs in the signaling of pathogens, abiotic stresses, plant hormones, and cell cycle cues. A large number of distinct MAPKs in plants have been identified that are all most similar to the animal ERK MAPKs. By sequence alignment all available full length plant MAPKs can be grouped into five subfamilies. Functional data exist for members of four subfamilies and show that different subfamilies encode MAPKs for specific functions. Analysis of partial MAPK sequences from full length, truncated cDNAs and expressed sequence tags (ESTs) revealed the presence of two new subfamilies in the plant MAPK superfamily. Signature sequences valid for the superfamily of plant MAPKs and each subfamily were derived and should help in future classification of novel MAPKs. The future challenge is to unambiguously assign functions to each MAPK and decipher the other partners of their signaling pathways.


Assuntos
Sistema de Sinalização das MAP Quinases/fisiologia , Proteínas Quinases Ativadas por Mitógeno/genética , Proteínas Quinases Ativadas por Mitógeno/metabolismo , Fenômenos Fisiológicos Vegetais , Regulação da Expressão Gênica de Plantas , Dados de Sequência Molecular , Homologia de Sequência de Aminoácidos
7.
Plant J ; 20(4): 381-8, 1999 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-10607291

RESUMO

Plant growth is severely affected by hyper-osmotic salt conditions. Although a number of salt-induced genes have been isolated, the sensing and signal transduction of salt stress is little understood. We provide evidence that alfalfa cells have two osmo-sensing protein kinase pathways that are able to distinguish between moderate and extreme hyper-osmotic conditions. A 46 kDa protein kinase was found to be activated by elevated salt concentrations (above 125 mM NaCl). In contrast, at high salt concentrations (above 750 mM NaCl), a 38 kDa protein kinase, but not the 46 kDa kinase, became activated. By biochemical and immunological analysis, the 46 kDa kinase was identified as SIMK, a member of the family of MAPKs (mitogen-activated protein kinases). SIMK is not only activated by NaCl, but also by KCl and sorbitol, indicating that the SIMK pathway is involved in mediating general hyper-osmotic conditions. Salt stress induces rapid but transient activation of SIMK, showing maximal activity between 8 and 16 min before slow inactivation. When inactive, most mammalian and yeast MAPKs are cytoplasmic but undergo nuclear transloca- tion upon activation. By contrast, SIMK was found to be a constitutively nuclear protein and the activity of the kinase was not correlated with changes in its intra-cellular compartmentation, suggesting an intra-nuclear mechanism for the regulation of SIMK activity.

8.
Cell Mol Life Sci ; 55(2): 204-13, 1999 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-10188583

RESUMO

Mitogen-activated protein kinase (MAPK) pathways are modules involved in the transduction of extracellular signals to intracellular targets in all eukaryotes. Distinct MAPK pathways are regulated by different extracellular stimuli and are implicated in a wide variety of biological processes. In plants there is evidence for MAPKs playing a role in the signaling of abiotic stresses, pathogens and plant hormones. The large number and divergence of plant MAPKs indicates that this ancient mechanism of bioinformatics is extensively used in plants and may provide a new molecular handle on old questions.


Assuntos
Proteínas Quinases Dependentes de Cálcio-Calmodulina/metabolismo , Fenômenos Fisiológicos Vegetais , Transdução de Sinais , Sequência de Aminoácidos , Dados de Sequência Molecular
9.
Science ; 276(5321): 2054-7, 1997 Jun 27.
Artigo em Inglês | MEDLINE | ID: mdl-9197271

RESUMO

Parsley cells recognize the fungal plant pathogen Phytophthora sojae through a plasma membrane receptor. A pathogen-derived oligopeptide elicitor binds to this receptor and thereby stimulates a multicomponent defense response through sequential activation of ion channels and an oxidative burst. An elicitor-responsive mitogen-activated protein (MAP) kinase was identified that acts downstream of the ion channels but independently or upstream of the oxidative burst. Upon receptor-mediated activation, the MAP kinase is translocated to the nucleus where it might interact with transcription factors that induce expression of defense genes.


Assuntos
Proteínas Quinases Dependentes de Cálcio-Calmodulina/metabolismo , Proteínas Fúngicas/farmacologia , Glicoproteínas de Membrana/farmacologia , Plantas/enzimologia , Sequência de Aminoácidos , Anfotericina B/farmacologia , Antracenos/farmacologia , Proteínas Quinases Dependentes de Cálcio-Calmodulina/química , Proteínas Quinases Dependentes de Cálcio-Calmodulina/genética , Núcleo Celular/enzimologia , Células Cultivadas , Ativação Enzimática , Canais Iônicos/efeitos dos fármacos , Canais Iônicos/metabolismo , Dados de Sequência Molecular , Oniocompostos/farmacologia , Fragmentos de Peptídeos/farmacologia , Fosforilação , Phytophthora/metabolismo , Plantas/genética , Plantas/microbiologia , Explosão Respiratória/efeitos dos fármacos
10.
Plant Cell ; 9(1): 75-83, 1997 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-12237344

RESUMO

Mechanical injury in plants induces responses that are involved not only in healing but also in defense against a potential pathogen. To understand the intracellular signaling mechanism of wounding, we have investigated the involvement of protein kinases. Using specific antibodies, we showed that wounding alfalfa leaves specifically induces the transient activation of the p44MMK4 kinase, which belongs to the family of mitogen-activated protein kinases. Whereas activation of the MMK4 pathway is a post-translational process and was not blocked by [alpha]-amanitin and cycloheximide, inactivation depends on de novo transcription and translation of a protein factor(s). After wound-induced activation, the MMK4 pathway was subject to a refractory period of 25 min, during which time restimulation was not possible, indicating that the inactivation mechanism is only transiently active. After activation of the p44MMK4 kinase by wounding, transcript levels of the MMK4 gene increased, suggesting that the MMK4 gene may be a direct target of the MMK4 pathway. In contrast, transcripts of the wound-inducible MsWIP gene, encoding a putative proteinase inhibitor, were detected only several hours after wounding. Abscisic acid, methyl jasmonic acid, and electrical activity are known to mediate wound signaling in plants. However, none of these factors was able to activate the p44MMK4 kinase in the absence of wounding, suggesting that the MMK4 pathway acts independently of these signals.

11.
Proc Natl Acad Sci U S A ; 93(20): 11274-9, 1996 Oct 01.
Artigo em Inglês | MEDLINE | ID: mdl-8855346

RESUMO

Yeast and animals use mitogen-activated protein (MAP) kinase cascades to mediate stress and extracellular signals. We have tested whether MAP kinases are involved in mediating environmental stress responses in plants. Using specific peptide antibodies that were raised against different alfalfa MAP kinases, we found exclusive activation of p44MMK4 kinase in drought- and cold-treated plants. p44MMK4 kinase was transiently activated by these treatments and was correlated with a shift in the electrophoretic mobility of the p44MMK4 protein. Although transcript levels of the MMK4 gene accumulated after drought and cold treatment, no changes in p44MMK4 steady state protein levels were observed, indicating a posttranslational activation mechanism. Extreme temperatures, drought, and salt stress are considered to be different forms of osmotic stress. However, high salt concentrations or heat shock did not induce activation of p44MMK4, indicating the existence of distinct mechanisms to mediate different stresses in alfalfa. Stress adaptation in plants is mediated by abscisic acid (ABA)-dependent and ABA-independent processes. Although ABA rapidly induced the transcription of an ABA-inducible marker gene, MMK4 transcript levels did not increase and p44MMK4 kinase was not activated. These data indicate that the MMK4 kinase pathway mediates drought and cold signaling independently of ABA.


Assuntos
Proteínas Quinases Dependentes de Cálcio-Calmodulina/genética , Proteínas Quinases Dependentes de Cálcio-Calmodulina/fisiologia , Regulação da Expressão Gênica de Plantas , Medicago sativa/genética , Proteínas Quinases Ativadas por Mitógeno , Sequência de Bases , Clonagem Molecular , Temperatura Baixa , Genes de Plantas , Técnicas Imunológicas , Dados de Sequência Molecular , Peptídeos/química , Peptídeos/imunologia , Proteínas de Plantas , RNA Mensageiro/genética , Transdução de Sinais , Equilíbrio Hidroeletrolítico
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