Photomorphogenesis is repressed in the dark mainly by an E3 ubiquitin ligase complex comprising CONSTITUTIVE PHOTOMORPHOGENIC 1 (COP1) and four homologous proteins called SUPPRESSOR OF PHYA‐105 (SPA1–SPA4) in Arabidopsis. This complex induces the ubiquitination and subsequent degradation of positively acting transcription factors (TFs; e.g. ELONGATED HYPOCOTYL (HY5), LONG HYPOCOTYL IN FAR‐RED 1 (HFR1), PRODUCTION OF ANTHOCYANIN PIGMENT 1 (PAP1) and others] in the dark to repress photomorphogenesis. Genomic evidence showed a large number of genes regulated by COP1 in the dark, of which many are direct targets of HY5. However, the genomic basis for the constitute photomorphogenic phenotype of
Light signal provides the spatial and temporal information for plants to adapt to the prevailing environmental conditions. Alterations in light quality and quantity can trigger robust changes in global gene expression. In
- NSF-PAR ID:
- 10248232
- Publisher / Repository:
- Wiley-Blackwell
- Date Published:
- Journal Name:
- The Plant Journal
- Volume:
- 96
- Issue:
- 2
- ISSN:
- 0960-7412
- Page Range / eLocation ID:
- p. 260-273
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
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spaQ remains unknown. Here, we show that >7200 genes are differentially expressed in thespaQ background compared to wild‐type in the dark. Comparison of the RNA sequencing (RNA‐Seq) data betweencop1 andspaQ revealed a large overlapping set of genes regulated by the COP1–SPA complex. In addition, many of the genes coordinately regulated by the COP1–SPA complex are also regulated by HY5 directly and indirectly. Taken together, our data reveal that SPA proteins repress photomorphogenesis by controlling gene expression in concert with COP1, likely through regulating the abundance of downstream TFs in light signaling pathways. Moreover, SPA proteins may function both in a COP1‐dependent and ‐independent manner in regulating many biological processes and developmental pathways in Arabidopsis. -
Abstract SAMHD 1 possesses multiple functions, but whether cellular factors regulateSAMHD 1 expression or its function remains not well characterized. Here, by investigating why culturedRD andHEK 293T cells show different sensitivity to enterovirus 71 (EV71) infection, we demonstrate thatSAMHD 1 is a restriction factor for EV71. Importantly, we identifyTRIM 21, an E3 ubiquitin ligase, as a key regulator ofSAMHD 1, which specifically interacts and degradesSAMHD 1 through the proteasomal pathway. However,TRIM 21 has no effect on EV71 replication itself. Moreover, we prove that interferon production stimulated by EV71 infection induces increasedTRIM 21 andSAMHD 1 expression, whereas increasingTRIM 21 overridesSAMHD 1 inhibition of EV71 in cells and in a neonatal mouse model.TRIM 21‐mediated degradation ofSAMHD 1 also affectsSAMHD 1‐dependent restriction ofHIV ‐1 and the regulation of interferon production. We further identify the functional domains inTRIM 21 required forSAMHD 1 binding and the ubiquitination site K622 inSAMHD 1 and show that phosphorylation ofSAMHD 1 at T592 also blocks EV71 restriction. Our findings illuminate how EV71 overcomesSAMHD 1 inhibition via the upregulation ofTRIM 21. -
Premise Light is critical in the ability of plants to accumulate chlorophyll. When exposed to far‐red (
FR ) light and then grown in white light in the absence of sucrose, wild‐type seedlings fail to green in a response known as theFR block of greening (BOG ). This response is controlled by phytochrome A through repression of protochlorophyllide reductase‐encoding (POR ) genes byFR light coupled with irreversible plastid damage. Sigma (SIG ) factors are nuclear‐encoded proteins that contribute to plant greening and plastid development through regulating gene transcription in chloroplasts and impacting retrograde signaling from the plastid to nucleus.SIG s are regulated by phytochromes, and the expression of someSIG factors is reduced in phytochrome mutant lines, includingphyA . Given the association of phyA with theFR BOG and its regulation ofSIG factors, we investigated the potential regulatory role ofSIG factors in theFR BOG response.Methods We examined
FR BOG responses insig mutants, phytochrome‐deficient lines, and mutant lines for several phy‐associated factors. We quantified chlorophyll levels and examined expression of keyBOG ‐associated genes.Results Among six
sig mutants, only thesig6 mutant significantly accumulated chlorophyll afterFR BOG treatment, similar to thephyA mutant.SIG 6 appears to control protochlorophyllide accumulation by contributing to the regulation of tetrapyrrole biosynthesis associated with glutamyl‐tRNA reductase (HEMA 1) function, select phytochrome‐interacting factor genes (PIF4 andPIF6 ), andPENTA1 , which regulatesPORA mRNA translation afterFR exposure.Conclusions Regulation of
SIG6 plays a significant role in plant responses toFR exposure during theBOG response. -
Summary Faithful chromosome segregation is required for both mitotic and meiotic cell divisions and is regulated by multiple mechanisms including the anaphase‐promoting complex/cyclosome (
APC /C), which is the largest known E3 ubiquitin‐ligase complex and has been implicated in regulating chromosome segregation in both mitosis and meiosis in animals. However, the role of theAPC /C during plant meiosis remains largely unknown. Here, we show that Arabidopsis is required for male meiosis.APC 8We used a combination of genetic analyses, cytology and immunolocalisation to define the function of At
APC 8 in male meiosis.Meiocytes from
apc8‐1 plants exhibit several meiotic defects including improper alignment of bivalents at metaphase I, unequal chromosome segregation during anaphaseII , and subsequent formation of polyads. Immunolocalisation using an antitubulin antibody showed thatAPC 8 is required for normal spindle morphology. We also observed mitotic defects inapc8‐1, including abnormal sister chromatid segregation and microtubule morphology.Our results demonstrate that Arabidopsis
APC /C is required for meiotic chromosome segregation and thatAPC /C‐mediated regulation of meiotic chromosome segregation is a conserved mechanism among eukaryotes. -
Summary The collaborative non‐self‐recognition model for S‐
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