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Congress Abstracts - Society for Developmental Biology

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downregulated by polycomb-group proteins, and that such regulation is suppressed after a vernalization treatment. Polycomb-group<br />

protein CLF methylates chromatin in the AGL19 locus, with the first intron being the most frequent target. Thus, it has been proposed<br />

that CLF jointly with other PRC2 proteins silences AGL19 expression by methylation. It is not known if this silencing occurs in the<br />

root, the organ where AGL19 shows the highest expression. On the other hand, our data from fusions of AGL19 promotor region and<br />

reporter genes suggests that AGL19 is upregulated by auxin. Studies on CLF mutants show that its role in the RAM is not linked to<br />

changes in auxin concentration. Based on this data, we ask ourselves whether the AGL19 regulatory pathway involving polycombgroup<br />

proteins and the one involving auxin are connected. In this work we characterized AGL19 molecular and cellular functions<br />

through analysis of a loss-of-function mutant. We found that AGL19 silencing by polycomb-group proteins also occurs in the root.<br />

Finally, we propose experiments involving auxin induction of AGL19 expression in CLF and LHP1 mutants in order to find out<br />

whether its epigenetic regulation is independent to auxin regulation.<br />

This work is supported by CONACyT (180098; 180380; 167705; 152649; 105678) and DGAPA, UNAM (IN204011-3; IN203113-3;<br />

IN226510-3; IB201212-2) grants.<br />

Program/Abstract # 135<br />

The SWI2/SNF2 Chromatin Remodeling Factor CHR9 Regulates Floral Meristem Identity in Cooperation with LEAFY<br />

Lamb, Rebecca S.; Kovach, Jeffrey; Habina, Matthew; Siriwardana, Nirodhini (Ohio State University, USA)<br />

In angiosperms the flower is the unit of reproduction and is considered to be a modified shoot. The floral meristem identity genes are<br />

required to specify meristems as flowers rather than as shoots. In the model plant species Arabidopsis thaliana as well as other<br />

flowering plants the LEAFY (LFY) transcription factor is a key regulator of floral development, regulating expression of other floral<br />

meristem identity genes and floral homeotic genes that control floral organ identity. We have identified CHR9, a member of the<br />

SWI2/SNF2 family of chromatin remodeling factors, as an LFY-interacting protein. chr9 loss-of-function mutations have mild<br />

meristem identity defects while CHR9 overexpression lines flower early with shoots converted to flowers. Physical and genetic<br />

interactions between LFY and CHR9 indicate that these factors act together. Evidence will be presented that CHR9 acts with LFY to<br />

regulate expression of floral meristem identity genes, including TERMINAL FLOWER 1 (TFL1), and thus CHR9 is involved in the<br />

control of plant reproductive architecture.<br />

Program/Abstract # 136<br />

Paternal contributions to early embryogenesis of Arabidopsis thaliana: A functional genetic approach<br />

Del Toro, Gerardo Del Toro; García-Aguilar, Marcelina; Gillmor, Stewart (CINVESTAV-IPN, Mexico)<br />

In animals, zygotic genome activation and maternal product decay are prerequisites <strong>for</strong> transfer of developmental control from the<br />

mother to the zygote, a phenomenon known as the Maternal to Zygotic Transition (MZT). In plants, the existence of a MZT is<br />

controversial. Two recent studies have reported allele-specific transcriptome profiles of early embryogenesis, one providing support<br />

<strong>for</strong> maternal dominance with significant paternal input (Autran et al., Cell 2011), and the other study arguing <strong>for</strong> equivalent parental<br />

contribution (Nodine and Bartel, Nature 2012). However, neither study tested the biological relevance of this phenomenon. Here we<br />

report the first systematic functional genetic analysis of paternal gene activity in early plant embryogenesis. Our assay consists of<br />

testing the timing of the ability of wild type paternal alleles to complement pre-globular embryo phenotypes conditioned by mutant<br />

maternal alleles. In our analysis of 50 embryo defective mutants (emb), we found that 82% of genes showed delayed<br />

complementation, while 18% showed immediate complementation. In addition, we used GCT/MED13 and CCT/MED12, two genes<br />

that show delayed phenotypic complementation, to correlate delayed paternal function with delayed paternal expression. Thus,<br />

activation of many paternal alleles in early embryogenesis is gradual, while a significant proportion of paternal alleles show<br />

immediate activity. Our results demonstrate that plants do not have discrete step <strong>for</strong> zygotic gene activation, and suggest that the<br />

maternal and paternal genomes make unequal contributions to early plant embryogenesis.<br />

Program/Abstract # 137<br />

Expression of Aminopeptidase N Genes During Sea Urchin Development<br />

Ingersoll, Eric P.; Drab, Diana L. (Penn State, USA)<br />

Aminopeptidase N (APN) is an exopeptidase that has been shown to play a role in the development of nematodes and fruit files.<br />

Recent advances in genome sequencing have made available in<strong>for</strong>mation allowing the identification of genes in the sea urchin<br />

genome. We have searched the sea urchin genome and found a number of APN genes. In this study, we are determining which of<br />

these APN genes is expressed during embryonic development. We used reverse transcription PCR to detect gene-specific mRNAs<br />

throughout development. Our studies have identified several APN genes that are expressed in embryos. We will present data on the<br />

temporal expression of these genes throughout the entirety of sea urchin embryonic development. In the future, we hope to determine<br />

the spatial expression patterns and developmental functions of these genes.<br />

Program/Abstract # 138<br />

Repulsive guidance molecules expression pattern during chicken embryogenesis suggested new roles <strong>for</strong> these molecules<br />

during notochord <strong>for</strong>mation, somitogenesis and myogenesis<br />

Jorge, Erika; Ahmed, Mohi (Mount Sinai School of Medicine, USA); Bothe, Ingo (Sloan Kettering Institute, USA); Coutinho, Luiz<br />

(Universidade de São Paulo, Brazil); Dietrich, Susanne (University of Portsmouth, UK)<br />

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