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1.
Plant Biotechnol J ; 13(5): 689-99, 2015 Jun.
Artículo en Inglés | MEDLINE | ID: mdl-25487628

RESUMEN

HUB1, also known as Ubl5, is a member of the subfamily of ubiquitin-like post-translational modifiers. HUB1 exerts its role by conjugating with protein targets. The function of this protein has not been studied in plants. A HUB1 gene, LpHUB1, was identified from serial analysis of gene expression data and cloned from perennial ryegrass. The expression of this gene was reported previously to be elevated in pastures during the summer and by drought stress in climate-controlled growth chambers. Here, pasture-type and turf-type transgenic perennial ryegrass plants overexpressing LpHUB1 showed improved drought tolerance, as evidenced by improved turf quality, maintenance of turgor and increased growth. Additional analyses revealed that the transgenic plants generally displayed higher relative water content, leaf water potential, and chlorophyll content and increased photosynthetic rate when subjected to drought stress. These results suggest HUB1 may play an important role in the tolerance of perennial ryegrass to abiotic stresses.


Asunto(s)
Regulación de la Expresión Génica de las Plantas , Lolium/genética , Proteínas de Plantas/metabolismo , Ubiquitina/metabolismo , Secuencia de Bases , Clorofila/metabolismo , Sequías , Expresión Génica , Lolium/fisiología , Datos de Secuencia Molecular , Hojas de la Planta/genética , Hojas de la Planta/fisiología , Proteínas de Plantas/genética , Plantas Modificadas Genéticamente , Análisis de Secuencia de ADN , Estrés Fisiológico , Ubiquitina/genética , Agua/fisiología
2.
Plant Biotechnol J ; 5(1): 146-61, 2007 Jan.
Artículo en Inglés | MEDLINE | ID: mdl-17207264

RESUMEN

Perennial ryegrass (Lolium perenne L.) is a major grass species used for forage and turf throughout the world, and gains by conventional breeding have reached a plateau. Perennial ryegrass is an outcrossing, self-incompatible diploid (2n = 2x = 14) with a relatively large genome (4067 Mbp/diploid genome; Evans, G.M., Rees, H., Snell, C.L. and Sun, S. (1972) The relation between nuclear DNA amount and the duration of the mitotic cycle. Chrom. Today, 3, 24-31). Using tissues sourced from active pastures during the peak of the autumn, winter, spring and summer seasons, we analysed the ryegrass transcriptome employing a Serial Analysis of Gene Expression (SAGE) protocol, with the dual goals of understanding the seasonal changes in perennial ryegrass gene expression and enhancing our ability to select genes for genetic manipulation. A total of 159,002 14-mer SAGE tags was sequenced and mapped to the perennial ryegrass DNA database, comprising methyl-filtered (GeneThresher) and expressed sequence tag (EST) sequences. The analysis of 14,559 unique SAGE tags, which were present more than once in our SAGE library, revealed 964, 1331, 346 and 131 exclusive transcripts to autumn, winter, spring and summer, respectively. Intriguingly, our analysis of the SAGE tags revealed season-specific expression profiles for the small subunit of ribulose-1,5-bisphosphate carboxylase (Rubisco), LprbcS. The transcript level for LprbcS was highest in spring, and then decreased gradually between summer and winter. Five different copies of LprbcS were revealed in ryegrass, with one possibly producing splice variant transcripts. Two highly expressed LprbcS genes were reported, one of which was not active in autumn. Another LprbcS gene showed an inverse expression profile to the autumn inactive LprbcS in a manner to compensate the expression level.


Asunto(s)
Perfilación de la Expresión Génica , Lolium/genética , Ribulosa-Bifosfato Carboxilasa/genética , Transcripción Genética , Empalme Alternativo , Etiquetas de Secuencia Expresada , Variación Genética , Genoma de Planta , Lolium/citología , Lolium/enzimología , Mitosis , Plantas Modificadas Genéticamente/enzimología , Estaciones del Año
3.
Nucleic Acids Res ; 31(1): 315-8, 2003 Jan 01.
Artículo en Inglés | MEDLINE | ID: mdl-12520011

RESUMEN

InterPro, an integrated documentation resource of protein families, domains and functional sites, was created in 1999 as a means of amalgamating the major protein signature databases into one comprehensive resource. PROSITE, Pfam, PRINTS, ProDom, SMART and TIGRFAMs have been manually integrated and curated and are available in InterPro for text- and sequence-based searching. The results are provided in a single format that rationalises the results that would be obtained by searching the member databases individually. The latest release of InterPro contains 5629 entries describing 4280 families, 1239 domains, 95 repeats and 15 post-translational modifications. Currently, the combined signatures in InterPro cover more than 74% of all proteins in SWISS-PROT and TrEMBL, an increase of nearly 15% since the inception of InterPro. New features of the database include improved searching capabilities and enhanced graphical user interfaces for visualisation of the data. The database is available via a webserver (http://www.ebi.ac.uk/interpro) and anonymous FTP (ftp://ftp.ebi.ac.uk/pub/databases/interpro).


Asunto(s)
Bases de Datos de Proteínas , Proteínas/química , Animales , Gráficos por Computador , Procesamiento Proteico-Postraduccional , Estructura Terciaria de Proteína , Proteínas/genética , Proteínas/metabolismo , Secuencias Repetitivas de Aminoácido , Interfaz Usuario-Computador
4.
Brief Bioinform ; 3(3): 225-35, 2002 Sep.
Artículo en Inglés | MEDLINE | ID: mdl-12230031

RESUMEN

The exponential increase in the submission of nucleotide sequences to the nucleotide sequence database by genome sequencing centres has resulted in a need for rapid, automatic methods for classification of the resulting protein sequences. There are several signature and sequence cluster-based methods for protein classification, each resource having distinct areas of optimum application owing to the differences in the underlying analysis methods. In recognition of this, InterPro was developed as an integrated documentation resource for protein families, domains and functional sites, to rationalise the complementary efforts of the individual protein signature database projects. The member databases - PRINTS, PROSITE, Pfam, ProDom, SMART and TIGRFAMs - form the InterPro core. Related signatures from each member database are unified into single InterPro entries. Each InterPro entry includes a unique accession number, functional descriptions and literature references, and links are made back to the relevant member database(s). Release 4.0 of InterPro (November 2001) contains 4,691 entries, representing 3,532 families, 1,068 domains, 74 repeats and 15 sites of post-translational modification (PTMs) encoded by different regular expressions, profiles, fingerprints and hidden Markov models (HMMs). Each InterPro entry lists all the matches against SWISS-PROT and TrEMBL (2,141,621 InterPro hits from 586,124 SWISS-PROT and TrEMBL protein sequences). The database is freely accessible for text- and sequence-based searches.


Asunto(s)
Biología Computacional , Bases de Datos de Proteínas , Proteínas , Algoritmos , Humanos , Servicios de Información , Internet , Proteínas/química , Proteínas/clasificación , Programas Informáticos
5.
Brief Bioinform ; 3(3): 285-95, 2002 Sep.
Artículo en Inglés | MEDLINE | ID: mdl-12230037

RESUMEN

The applications of InterPro span a range of biologically important areas that includes automatic annotation of protein sequences and genome analysis. In automatic annotation of protein sequences InterPro has been utilised to provide reliable characterisation of sequences, identifying them as candidates for functional annotation. Rules based on the InterPro characterisation are stored and operated through a database called RuleBase. RuleBase is used as the main tool in the sequence database group at the EBI to apply automatic annotation to unknown sequences. The annotated sequences are stored and distributed in the TrEMBL protein sequence database. InterPro also provides a means to carry out statistical and comparative analyses of whole genomes. In the Proteome Analysis Database, InterPro analyses have been combined with other analyses based on CluSTr, the Gene Ontology (GO) and structural information on the proteins.


Asunto(s)
Biología Computacional , Bases de Datos de Proteínas , Genoma , Proteínas , Proteoma/análisis , Secuencia de Aminoácidos , Genoma Humano , Humanos , Internet , Conformación Proteica , Proteínas/química , Proteínas/clasificación , Proteínas/genética , Proteínas/fisiología , Análisis de Secuencia de Proteína , Programas Informáticos
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