The over-expression of the anti-apoptotic Bcl-2 protein in lymphocytes
Cluster B contains only three sequences including a transmembrane Brefeldin A ARFs CLPTM1 family protein, which is also induced in response to bacterial infection and was identified as a possible downstream target of the heat shock regulator HsfA1a, and a putative Inhibitors,Modulators,Libraries pyridoxal biosynthesis pro tein PDX1. 1, which is essential for vitamin B6 biosynth esis and has been correlated to stress tolerance and photoprotection in Arabidopsis. Figure 5 shows the percentages of melon genes assigned different functional categories in clusters C and D. The Metabolism and Unknown protein categories are similarly represented in both clusters. Defense response transcripts are also similarly represented with 9% and 12% in clusters C and D, respectively.
The Response to stimulus and Secondary metabolism categories are well represented in Cluster C, each accounting for 7 8%, while in cluster D they only represent about 2% of TDFs. The Trans port category Inhibitors,Modulators,Libraries represents 1% of TDFs in C, but 5% in D. Identification of F. oxysporum f. sp. melonis genes expressed in melon during infection FOM genomic sequence data are scarce, so we expanded the search to include sequences from other Fusarium species or F. oxysporum formae speciales avail able in public databases. A total of 195 TDFs expressed Inhibitors,Modulators,Libraries in planta during the infection were identified as homo logous to sequences assigned to F. oxysporum f. sp. lyco persici, F. graminearum or F. verticilloides. Among these transcripts, 123 generated similar sized bands in the cDNA AFLP lanes of the fungal strains grown in vitro, while the remaining 72 fragments corresponded to transcripts that were not detected in fungal colonies but only in planta during the infection and may therefore represent factors related to virulence.
As expected, pathogen transcripts were detected predominantly during the late infection phase and almost exclusively in the compatible interac tion, probably due to the higher fungal biomass pro duced in host tissues. Selected FOM transcripts detected in Inhibitors,Modulators,Libraries planta are listed in Table 2. Fungal genes expressed only in planta or in planta and Inhibitors,Modulators,Libraries in vitro were also assigned functional categories based on careful literature evalua tion. This allowed us to identify some interesting differ ences, namely in the Cell component and in the Virulence categories, which are represented more in planta than in vitro. Other categories show similar per centages in both groups. Detection of fungal transcripts differentially expressed among strains grown in vitro We identified 199 bands that were differentially expressed among the three FOM strains grown in vitro, 75 of which were expressed uniquely in vitro and Axitinib supplier were selected for amplification and sequencing.