alate to oxa loacetate, and lipoamide to dihydrolipoamide interconversions, were dif ferentially expressed in all three backgrounds. Furthermore, ESTs associated with nine steps of glycolysis and exhibiting research use significant lowered expression patterns were identified. Phosphoglycerate mutase, pyruvate ferredoxin oxidoreductase, and dehydrolipoamide acetyltransferase were found in the o2 background only, pyru vate kinase and fructose biphosphate aldo lase were found in the o7 endosperm, while ESTs homologous to dehydrolipoamide dehydro genase, pyruvate dehydrogenase, and enolase exhibited a reduced expression in all three backgrounds. Furthermore, several genes involved in the redox status such as cytochrome C oxi dase reduction, thieredoxin and pyrophosphatase were strongly negatively affected in the opaque mutations, while a H transporting ATPase and a thiosulfate sulfur transferase were greatly increased in o2 and o7 endo sperms, respectively.

Starch metabolism Our profiling assays identified six differentially expressed ESTs exhibiting sequence homology with starch and sucrose metabolism related enzymes. ESTs homologous to enzymes catalyzing the inter conversion from a D glucose 6P into Inhibitors,Modulators,Libraries a D glucose 1P, from a D glucose 1P into ADP glucose, from ADP glucose into starch and from amylose into amylopectin were down regulated in expression in the o2 background only. UDP glucose to sucrose conversion appeared down regulated in the o7 background, while UDP glucose to sucrose 6P conversion appeared down regulated in all three backgrounds.

Storage protein synthesis As expected, storage protein Inhibitors,Modulators,Libraries Inhibitors,Modulators,Libraries synthesis was greatly affected in the mutant backgrounds analyzed. In the o2 background, a reduction of the 22 kDa a zein transcrip tion pool was observed, while a concomitant increase of 10, and 50 kDa g zein transcripts was seen. The o7 endosperm showed a marked reduction of 19 kDa a zein transcription levels, as well as a reduction of 10, 27, and 50 kDa g zeins. The transcription level of the 18 kDa zein class appeared increased in this back ground. Finally, the o2o7 endosperm showed a reduced transcription level of the 10 kDa g, 19 and 22 kDa a, and 27 and 50 kDa g zein gene pools. A series of ESTs homologous to genes involved in gene transcription Inhibitors,Modulators,Libraries and translation processes showed variation in the expression patterns analyzed.

In particular, three putative MADS box domain transcription factors GSK-3 were identified in the o2 background as well as two G box binding factors and a YABBY2 factor, a member of the YABBY family of TFs, were down regulated in o2. The o7 endosperm showed differential expression of a putative MADS box gene, a putative MYB family transcription factor and a homologue of the Ponatinib Bcr-Abl inhibitor OCL5 DNA binding homeobox protein. It was interesting to note that in the o7 endosperm mutant the expression of the transcriptional regulator O2 is significantly down regulated. Additionally, ESTs homologous to the JAB1 protein and to a putative G box binding factor showed alter