4 research outputs found
Analysis of the leaf transcriptome of Musa acuminata during interaction with Mycosphaerella musicola: gene assembly, annotation and marker development
Expressed sequence tags from the plant trypanosomatid phytomonas serpens
We have generated 2190 expressed sequence tags (ESTs) from a cDNA library of the plant trypanosomatid Phytomonas serpens. Upon processing and clustering the set of 1893 accepted sequences was reduced to 697 clusters consisting of 452 singletons and 245 contigs. Functional categories were assigned based on BLAST searches against a database of the eukaryotic orthologous groups of proteins (KOG). Thirty six percent of the generated sequences showed no hits against the KOG database and 39.6% presented similarity to the KOG classes corresponding to translation, ribosomal structure and biogenesis. The most populated cluster contained 45 ESTs homologous to members of the glucose transporter family. This fact can be immediately correlated to the reported Phytomonas dependence on anaerobic glycolytic ATP production due to the lack of cytochrome-mediated respiratory chain. In this context, not only a number of enzymes of the glycolytic pathway were identified but also of the Krebs cycle as well as specific components of the respiratory chain. The data here reported, including a few hundred unique sequences and the description of tandemly repeated motifs and putative transcript stability motifs at untranslated mRNA ends, represent an initial approach to overcome the lack of information on the molecular biology of this organism
High-throughput gene and SNP discovery in ucalyptus grandis, an uncharacterized genome
With the purpose of generating the first broad survey of gene sequences in Eucalyptus grandis, the most widely planted hardwood tree species, we used 454 technology to sequence and assemble 148 Mbp of expressed sequences (EST). EST sequences were generated from a normalized cDNA pool comprised of multiple tissues and genotypes, promoting discovery of homologues to almost half of Arabidopsis genes, and a comprehensive survey of allelic variation in the transcriptome. By aligning the sequencing reads from multiple genotypes we detected 23,742 SNPs, 83% of which were validated in a sample. Genome-wide nucleotide diversity was estimated for 2,392 contigs using a modified theta () parameter, adapted for measuring genetic diversity from polymorphisms detected by randomly sequencing a multigenotype cDNA pool. Diversity estimates in non-synonymous nucleotides were on average 4x smaller than in synonymous, suggesting purifying selection. Non-synonymous to synonymous substitutions (Ka/Ks) among 2,001 contigs averaged 0.30 and was skewed to the right, further supporting that most genes are under purifying selection. Comparison
of these estimates among contigs identified major functional classes of genes under purifying and diversifying selection in agreement with previous researches
A wor1-like transcription factor is essential for virulence of Cryptococcus neoformans
Gti1/Pac2 transcription factors occur exclusively in fungi and their roles vary according
to species, including regulating morphological transition and virulence, mating and
secondary metabolism. Many of these functions are important for fungal pathogenesis.
We therefore hypothesized that one of the two proteins of this family in Cryptococcus
neoformans, a major pathogen of humans, would also control virulence-associated
cellular processes. Elimination of this protein in C. neoformans results in reduced
polysaccharide capsule expression and defective cytokinesis and growth at 37◦C. The
mutant loses virulence in a mouse model of cryptococcal infection and retains only
partial virulence in the Galleria mellonella alternative model at 30◦C. We performed
RNA-Seq experiments on the mutant and found abolished transcription of genes that,
in combination, are known to account for all the observed phenotypes. The protein has
been named Required for cytokinesis and virulence 1 (Rcv1).Faculdade de Medicina (FMD)Faculdade UnB Ceilândia (FCE)Instituto de Ciências Biológicas (IB)Faculdade de Ciências da Saúde (FS)Departamento de Farmácia (FS FAR)Departamento de Biologia Celular (IB CEL