Characterization of a novel trithorax group gene candidate in Arabidopsis
dc.contributor.advisor
Goodrich, Justin
en
dc.contributor.advisor
Hudson, Andrew
en
dc.contributor.author
Liang, Shih-Chieh
en
dc.contributor.sponsor
Darwin Trust Scholarship
en
dc.date.accessioned
2016-11-11T09:36:50Z
dc.date.available
2016-11-11T09:36:50Z
dc.date.issued
2013-11-28
dc.description.abstract
The Polycomb group (Pc-G) and trithorax group (trx-G) genes play crucial roles in
development by regulating expression of homeotic and other genes that control cell fate.
Both groups catalyse modifications in chromatin, including histone methylation,
leading to epigenetic changes in gene activity. The trx-G antagonises the function of
Pc-G genes by activating Pc-G target genes, and consequently trx-G mutants suppress
Pc-G mutants. The trx-G genes are relatively poorly characterised in plants. We
identified a novel trx-G candidate SUPRESSOR OF POLYCOMB 12 (SOP12) by a
genetic screen for suppressors of mutants for the Arabidopsis Pc-G gene CURLY LEAF
(CLF). Thus sop12 mutations have no discernible phenotype in wild type backgrounds
but partially suppress the leaf curling and early flowering phenotypes of clf mutants.
Molecular cloning shows that SOP12 encodes a Harbinger transposase nuclease-like
protein which is conserved in green plants, although key residues required for the
catalytic activity of the nuclease domain are not conserved. In sop12 clf double mutants,
many CLF target genes are down-regulated relative to clf mutant, which suggests
SOP12 is a general activator of Pc-G target genes instead of a target of CLF or a late
flowering suppressor. The CLF gene encodes an H3K27me3 histone methyltransferase,
however chromatin immunoprecipitation (ChIP) analysis indicates that SOP12 does
not antagonise Pc-G by removing H3K27me3 methylation, which is consistent with the
fact that sop12 suppresses mutants for another Pc-G gene, LIKE
HETEROCHROMATIN PROTEIN 1 (LHP1), which is not involved in H3K27me3
deposition. Rather, genetic analysis shows that sop12 enhances the phenotype of
mutants of EARLY FLOWERING IN SHORT DAYS (EFS), a trx-G gene involved in
deposition of H3K36me3, and of ULTRAPETALA 1 (ULT1), a plant specific trx-G gene.
The enhancement indicates SOP12 may act together with ULT or EFS proteins, or at
least regulate the same targets in synergistic ways. For example, SOP12 activates AP3
expression, a role which overlaps with EFS. Yeast two hybrid screening and
imunoprecipitation followed by Mass spectrometry were performed to identify
numerous potential SOP12 interacting proteins but await further validation. One
protein (SUP1) identified through yeast two hybrid screens was independently
identified by another group as a Pc-G suppressor, suggesting that SOP12 and SUP1
may act in a common complex to regulate Pc-G targets.
Collectively, my data suggests
that SOP12 represents a domestic transposase that has acquired a role as a novel, plant
specific trx-G members.
en
dc.identifier.uri
http://hdl.handle.net/1842/17877
dc.language.iso
en
dc.publisher
The University of Edinburgh
en
dc.subject
Polycomb group
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dc.subject
trithorax group
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dc.subject
epigenetics
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dc.title
Characterization of a novel trithorax group gene candidate in Arabidopsis
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dc.type
Thesis or Dissertation
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dc.type.qualificationlevel
Doctoral
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dc.type.qualificationname
PhD Doctor of Philosophy
en
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