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399 Identification and Characterization of Sugar-Response Genes by Genomics and Reverse<br />

Genetics in Arabidopsis<br />

Chunyao Li, Tim Heisel, Sue Gibson<br />

Department of Plant Biology, University of Minnesota<br />

Sugars play a critical role in modulating plant development, metabolism and gene expression. In addition, sugarresponse<br />

pathways are thought to help regulate allocation of fixed carbon between source and sink tissues, and so play<br />

an important role in carbon partitioning and, ultimately, crop yields. Sugar signaling networks are also found to interact<br />

<strong>with</strong> phytohormone signaling networks, such as those regulated by abscisic acid, ethylene and gibberellins. Despite the<br />

importance of sugar-response pathways, only a small percentage of the components predicted to act in these pathways<br />

have been identified so far. We are employing an approach combining genomics and reverse genetics to identify and<br />

characterize genes that are involved in sugar response pathways. By analyzing Affymetrix GeneChip data we selected 189<br />

glucose- and/or sucrose-regulated genes that are predicted to encode proteins <strong>with</strong> activities commonly associated <strong>with</strong><br />

response pathways, such as transcription factors, protein kinases and protein phosphatases. We then identified T-DNA<br />

insertion lines that are homozygous for insertions in most of these 189 target genes. Currently we are screening these<br />

T-DNA insertion lines for defects in any of several sugar responses. To date we have identified two mutants, sov1 and<br />

hac1, that show altered sensitivity to the inhibitory effects of high concentrations of exogenous sugars on early seedling<br />

development. The sov1 mutant exhibits a hypersensitive response to the inhibitory effects of both sucrose and glucose<br />

during seed germination and early seedling development. In addition, sov1 is hypersensitive to the phytohormone abscisic<br />

acid. The hac1 mutant exhibits weak insensitivity to sucrose during seed germination and early seedling development.<br />

In addition to sov1 and hac1, we have also found that several other mutants exhibit alterations in sugar-regulated gene<br />

expression by real-time PCR analysis.<br />

400 Light regulation of gene expression in soybean<br />

Ying Li, Matthew Hudson<br />

University of Illinois at Urbana-Champaign<br />

Photomorphogenesis is relatively well understood in model systems like Arabidopsis. For example, the expression<br />

profiles of genes response to light signals in Arabidopsis have been examined in detail, using oligonucleotide microarrays.<br />

However, although the importance of photomorphogenic effects on crop morphology, physiology and yield are undoubted,<br />

photomorphogenic effects in crop plants are under-researched. In our study, we focused on the transcriptional regulation of<br />

photomorphogenesis in soybean using microarrays and real-time PCR. We used the soybean cDNA microarray developed<br />

by the NSF Soybean Functional Genomics project to find genes whose expression changes rapidly in etiolated soybean<br />

seedlings in response to a pulse of far red light. We then used published Arabidopsis microarray data to translate existing<br />

knowledge of photomorphogenesis into a better understanding of the mechanism of light-regulated development and signal<br />

transduction in soybean, and the natural variation in this process between soybean and Arabidopsis. We computationally<br />

determined the orthologous relationships between the genes represented on the NSF soybean cDNA microarray and the<br />

Arabidopsis oligonucleotide array, and compared the phytochrome regulated networks in soybean and Arabidopsis. Our<br />

results show that although some of the light regulated genes in the soybean microarray have orthologs in Arabidopsis, many<br />

are unique to soybean, suggesting overlapping and yet distinct transcriptional networks controlling photomorphogenesis<br />

in the two plant species. Results from this analysis will be presented.

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