Aphid biology: Expressed genes from alate Toxoptera citricida, the brown citrus aphid

The brown citrus aphid, Toxoptera citricida (Kirkaldy), is considered the primary vector of citrus tristeza virus, a severe pathogen which causes losses to citrus industries worldwide. The alate (winged) form of this aphid can readily fly long distances with the wind, thus spreading citrus tristeza virus in citrus growing regions. To better understand the biology of the brown citrus aphid and the emergence of genes expressed during wing development, we undertook a large-scale 5′ end sequencing project of cDNA clones from alate aphids. Similar large-scale expressed sequence tag (EST) sequencing projects from other insects have provided a vehicle for answering biological questions relating to development and physiology. Although there is a growing database in GenBank of ESTs from insects, most are from Drosophila melanogaster and Anopheles gambiae, with relatively few specifically derived from aphids. However, important morphogenetic processes are exclusively associated with piercing-sucking insect development and sap feeding insect metabolism. In this paper, we describe the first public data set of ESTs from the brown citrus aphid, T. citricida. The cDNA library was derived from alate adults due to their significance in spreading viruses (e.g., citrus tristeza virus). Over 5180 cDNA clones were sequenced, resulting in 4263 high-quality ESTs. Contig alignment of these ESTs resulted in 2124 total assembled sequences, including both contiguous sequences and singlets. Approximately 33% of the ESTs currently have no significant match in either the non-redundant protein or nucleic acid databases. Sequences returning matches with an E-value of ≤ −10 using BLASTX, BLASTN, or TBLASTX were annotated based on their putative molecular function and biological process using the Gene Ontology classification system. These data will aid research efforts in the identification of important genes within insects, specifically aphids and other sap feeding insects within the Order Hemiptera. The sequence data described in this paper have been submitted to Genbank's dbEST under the following accession numbers.: CB814527-CB814982, CB832665-CB833296, CB854878-CB855147, CB909714-CB910020, CB936196-CB936346, CD449954-CD450759. Abbreviation: / EST: expressed sequence ta

The Complete Nucleotide Sequence of the Coffee (Coffea Arabica L.) Chloroplast Genome: Organization and Implications for Biotechnology and Phylogenetic Relationships Amongst Angiosperms

The chloroplast genome sequence of Coffea arabica L., the first sequenced member of the fourth largest family of angiosperms, Rubiaceae, is reported. The genome is 155 189 bp in length, including a pair of inverted repeats of 25 943 bp. Of the 130 genes present, 112 are distinct and 18 are duplicated in the inverted repeat. The coding region comprises 79 protein genes, 29 transfer RNA genes, four ribosomal RNA genes and 18 genes containing introns (three with three exons). Repeat analysis revealed five direct and three inverted repeats of 30 bp or longer with a sequence identity of 90% or more. Comparisons of the coffee chloroplast genome with sequenced genomes of the closely related family Solanaceae indicated that coffee has a portion of rps19 duplicated in the inverted repeat and an intact copy of infA. Furthermore, whole-genome comparisons identified large indels (\u3e 500 bp) in several intergenic spacer regions and introns in the Solanaceae, including trnE (UUC)–trnT (GGU) spacer, ycf4–cemA spacer, trnI (GAU) intron and rrn5–trnR (ACG) spacer. Phylogenetic analyses based on the DNA sequences of 61 protein-coding genes for 35 taxa, performed using both maximum parsimony and maximum likelihood methods, strongly supported the monophyly of several major clades of angiosperms, including monocots, eudicots, rosids, asterids, eurosids II, and euasterids I and II. Coffea (Rubiaceae, Gentianales) is only the second order sampled from the euasterid I clade. The availability of the complete chloroplast genome of coffee provides regulatory and intergenic spacer sequences for utilization in chloroplast genetic engineering to improve this important crop

Desenvolvimento do limoeiro 'Volkameriano' (Citrus volkameriana Pasq.) submetido a doses de paclobutrazol e ácido giberélico

O trabalho foi desenvolvido com o objetivo de avaliar os efeitos de concentrações de paclobutrazol (PBZ) e ácido giberélico (GA3) sobre o desenvolvimento de plantas de limoeiro 'Volkameriano' cultivadas em sacolas plásticas, contendo 2,5 dm³ de substrato. O experimento foi montado em esquema fatorial 4x 2, sendo quatro concentrações de PBZ (0; 75; 150 e 225 mg do i.a. planta-1) e duas de GA3 (0 e 20 mg do i.a. L-1), no delineamento em blocos casualizados, com quatro repetições e cinco plantas por unidade experimental. Concentrações crescentes de PBZ reduziram o comprimento e diâmetro de caule, comprimento dos entrenós e área foliar, e aumentaram a massa foliar específica e as unidades SPAD. O GA3 reverteu a ação do PBZ. A aplicação de concentrações crescentes de PBZ, na presença de GA3, aumentou o diâmetro de caule até o valor máximo de 0,973 cm, que foi alcançado com a concentração estimada de 90,0 mg planta-1 de PBZ. O aumento das concentrações de PBZ não alterou o número de folhas, enquanto o GA3, na ausência do PBZ, aumentou em 10% o número de folhas e reduziu em 17,93% o comprimento de caule