Xu XM et al. (2009) Sheng Li Ke Xue Jin Zhan "[Physiological and molecular control of lipid accumulation in Caenorhabditis elegans]."

Wang DY, Xu XM

[Sheng Li Ke Xue Jin Zhan, 2009]

Fat storage is a complex physiological process, and model organism of Caenorhabditis elegans has already been explored as an important model to study lipid accumulation. The lipid particles or fatty acid can be stained or labeled with Sudan Black B or Neil Red. The metabolism pathways for fatty acid synthesis and breakdown in nematodes are almost identical to those in other organisms, and functions of many genes encoding the key regulation enzymes have been identified. At least four central regulation pathways are involved in the fat storage control in nematodes: insulin and TGF-beta signaling pathway, sbp-1/mdt-15 mediated pathway, nhr-49 mediated pathway, and TOR and hexosamine pathway. Moreover, neurotransmitters 5-HT, dopamine, and glutamate were found to participate in the control of lipid accumulation. In addition, involvement of tub-1 and bbs-1 in neuronal control of fat storage suggest the possibly important roles of amphid structure and sensory neurons in regulating lipid accumulation. The data obtained in C. elegans on fat storage control will contribute largely to the study on metabolism related diseases, such as obesity, in human beings.

Fire A et al. (1994) Worm Breeder's Gazette "Vectorology I: New lacZ Vectors (Building a Better Gene Trap)."

Fire A, Xu SQ

[Worm Breeder's Gazette, 1994]

Vectorology I: New lacZ vectors ("building a better gene trap") Andrew Fire and SiQun Xu Carnegie Institution of Washington, Baltimore, Md 21210

Hosono R et al. (2000) Japanese Worm Meeting "Characterization of a habituation contribution gene, hab-1"

Sassa T, Xu XM, Hosono R

[Japanese Worm Meeting, 2000]

C.elegans locomotes backward when given the single mechanical stimulation such as tap or touch at the anterior body region. When given repetitive these mechanical stimuli the response gradually attenuates and the animal falls into the habituated state. We found the acquisition of habituation is mediated by the specific neuron ( Kitamura et al., submitted to press). To find genes involved in the habituation behavior, we isolated mutants showing the tap mediated habituation abnormal. Mutation in hab-1, shows delay to acquire habituation and retention. The response of the hab-1 mutant (cn308) is normal for a single mechanical stimulation. The habituation phenotype of the mutant is also abnormal for the repetitive head, nose or tail touch. These results suggest that the mutant is not defective in specific habituation induced by repetitive tap stimuli but generally defective in habituation. We tested chemotaxis and adaptation to benzaldehyde, isoamylalcohol, diacetyl, pyrazine and butanone. The response to the reagents of the mutant were indistinguishable from that of the wild-type animals. We mapped hab-1 at the right hand of LGI in the vicinity of unc-100. By cosmid rescue experiments, six cosmid clones (K03D10, C15B2, ZK849, C49A1, K04H8, F09C3) were identified covering the hab-1 gene.

Niethammer P (2014) Dev Cell "Stress heals."

Niethammer P

[Dev Cell, 2014]

Reactive oxygen species (ROS) are generated as a response to cellular stress and regulate processes including cellular signaling and wound healing. In this issue of Developmental Cell, Xu and Chisholm (2014) demonstrate that mitochondrial ROS are required for proper wound healing in Caenorhabditis elegans through controlling the redox state of actin regulators.

Bonini NM (2001) Dev Cell "Stores to die for."

Bonini NM

[Dev Cell, 2001]

Genes that regulate apoptosis are well defined. In contrast, it has not been clear what genes are central to necrotic cell loss. In the September 27th issue of Neuron, Xu et al. (2001) report a critical role for genes that regulate storage and release of Ca2+ from the endoplasmic reticulum as important to necrotic-like cellular degeneration in Caenorhabditis elegans.

Fire A et al. (1998) Nature "Potent and specific genetic interference by double-stranded RNA in Caenorhabditis elegans."

Fire A, Mello CC, Kostas SA, Montgomery MK, Driver SE, Xu SQ

[Nature, 1998]

Experimental introduction of RNA into cells can be used in certain biological systems to interfere with the function of an endogenous gene. Such effects have been proposed to result from a simple antisense mechanism that depends on hybridization between the injected RNA and endogenous messenger RNA transcripts. RNA interference has been used in the nematode Caenorhabditis elegans to manipulate gene expression. Here we investigate the requirements for structure and delivery of the interfering RNA. To our surprise, we found that double-stranded RNA was substantially more effective at producing interference than was either strand individually. After injection into adult animals, purified single strands had at most a modest effect, whereas double-stranded mixtures caused potent and specific interference. The effects of this interference were evident in both the injected animals and their progeny. Only a few molecules of injected double-stranded RNA were required per affected cell, arguing against stochiometric interference with endogenous mRNA and suggesting that there could be a catalytic or amplification component in the interference process.AD - Carnegie Institution of Washington, Department of Embryology, Baltimore, Maryland 21210, USA. fire@mail1.ciwemb.eduFAU - Fire, AAU - Fire AFAU - Xu, SAU - Xu SFAU - Montgomery, M KAU - Montgomery MKFAU - Kostas, S AAU - Kostas SAFAU - Driver, S EAU - Driver SEFAU - Mello, C CAU - Mello CCLA - engPT - Journal ArticleCY - ENGLANDTA - NatureJID - 0410462RN - 0 (Calmodulin-Binding Proteins)RN - 0 (Helminth Proteins)RN - 0 (Muscle Proteins)RN - 0 (RNA, Antisense)RN - 0 (RNA, Double-Stranded)RN - 0 (twitchin)SB - IM

SN Parrish et al. (1999) International C. elegans Meeting "Investigating the fates of trigger RNAs and target transcripts in RNA-mediated interference"

AZ Fire, SN Parrish

[International C. elegans Meeting, 1999]

We seek to explore the molecular mechanisms responsible for RNA-mediated genetic interference (RNAi). In nematodes, introduction of double-stranded RNA corresponding to a segment of an endogenous genetic locus can result in specific silencing of that locus, essentially producing a knock out phenotype [1]. To date, evidence indicates that this interference reflects a post-transcriptional mechanism, resulting in the loss of the endogenous transcript [2]. Only a few molecules of dsRNA are required per cell to mediate interference, suggesting either an amplification or catalytic aspect of the process [1]. To gain an understanding of the mechanism of RNAi, we are examining the fates of the two key players in this pathway, the endogenous target RNA and the dsRNA effector molecule. First, we are attempting to follow alterations in the endogenous transcripts after the introduction of dsRNA. As a start, we are trying to map possible cleavage events or potential chemical modifications through primer extension and RT PCR of the target transcript. In a complementary set of experiments, we are also examining potential changes in the dsRNA triggering molecule. Through the characterization of the target and effector RNA molecules, we hope to acquire some insight into the mechanism of RNA-triggered silencing. With this knowledge, in conjunction with genetic identification of components in the pathway, it may be possible to unravel the events and intermediates essential for RNAi. 1. Fire, Xu, Montgomery, Kostas, Driver, Mello. Nature 391, 806 2. Montgomery, Xu, and Fire. PNAS 95, 15502

Gladyshev VN et al. (1999) Biochem Biophys Res Commun "Selenocysteine-containing thioredoxin reductase in C. elegans."

Wootton JC, Hatfield DL, Lee BJ, Korotkov KV, Krause MW, Xu XM, Sun QA, Gladyshev VN, Kryukov GV

[Biochem Biophys Res Commun, 1999]

Mammalian thioredoxin reductases contain a TGA-encoded C-terminal penultimate selenocysteine (Sec) residue, and show little homology to bacterial, yeast, and plant thioredoxin reductases. Here we show that the nematode, Caenorhabditis elegans, contains two homologs related to the mammalian thioredoxin reductase family. The gene for one of these homologs contains a cysteine codon in place of TGA, and its product, designated TR-S, was previously suggested to function as thioredoxin reductase. The other gene contains TGA and its product is designated TR-Se. This Sec-containing thioredoxin reductase lacks a canonical Sec insertion sequence element in the 3'-untranslated area of the gene. TR-Se shows greater sequence similarity to mammalian thioredoxin reductase isozymes TR1 and TR2, whereas TR-S is more similar to TR3. TR-Se was identified as a thioredoxin reductase selenoprotein by labeling C. elegans with 75Se and characterizing the resulting 75Se-labeled protein by affinity and other column chromatography and gel-electrophoresis. TR-Se was expressed in Escherichia coli as a selenoprotein when a bacterial SECIS element was introduced downstream of the Sec TGA codon. The data show that TR-Se is the major naturally occurring selenoprotein in C. elegans, and suggest an important role for selenium and the thioredoxin system in this organism.

Hung, Wesley L. et al. (2019) International Worm Meeting "A compact circuit of interneurons coordinates two central pattern generators to control forward movement."

Sathaseevan, Anson, Meng, Jun, Zhen, Mei, Chang, Maggie M., Hung, Wesley L., Miller III, David M., Lu, Yangning, Wang, Ying, McWhirter, Rebecca, Luo, Linjiao

[International Worm Meeting, 2019]

In C. elegans, there are two central pattern generators (CPGs) that contribute to forward movement - the head CPG that controls the head swing, through currently unidentified neurons, and the body CPGs, which resides in the B-type motor neurons (Xu et al., 2017). The frequency and amplitude of the head swing and body undulation are tightly coupled to allow smooth, sinusoidal forward movement. We show here that the descending interneurons, AVG and RIF, play a critical role in two aspects of forward movement: forward speed modulation and head-body coordination. While AVG is not essential for locomotion, the loss of AVG results in animals with reduced forward speed and an increased tendency to remain in a pausing/resting state. Conversely, optogenetic activation of AVG alone rapidly increases forward velocity. This effect requires gap junction-mediated activation of RIFL/R, which subsequently activates the premotor interneurons AVBL/R to increase activity of the forward movement-driving B motor neurons. When head swinging is inhibited, body undulation is decreased. Conversely, increased head swinging frequency leads to increased body undulation frequency to potentiate higher forward velocity. This suggests communication between the head and body CPGs. Our preliminary results suggest that AVG may also be required to coordinate the head and body CPGs. Activation of AVG was sufficient to drive body bends even when head swinging was inhibited. Increased head swinging is not able change body undulation when AVG is ablated. We propose that the descending interneuron circuit (AVG-RIF-AVB) permits generation of adaptive forward movement by modulating forward speed and linking the head and body CPGs. Xu, T. et. al. PNAS May 8, 2018 115 (19) E4493-E4502

Voia, Anna et al. (2022) MicroPubl Biol

Labbe, Jean-Claude, Voia, Anna, Poupart, Vincent

[MicroPubl Biol, 2022]

Plants of the Mimosa genus are studied and used for their bioactive properties. Among bioactive phytochemicals are quercetin and myricetin, which have been demonstrated to act as antioxidants in many contexts (Taheri et al. 2020; Xu et al. 2019), including in C. elegans (Buchter et al. 2013; Grnz et al. 2012; Sugawara and Sakamoto 2020). Other phytochemicals from these plants, such as the triterpenoid phytosterol lupeol, have been shown to have antioxidant properties but have not been as extensively characterized in model organisms (Liu et al. 2021; Shai et al. 2009). Here we employed the nematode C. elegans to assess whether lupeol elicits antioxidant response in vivo . Using reporter assays for oxidative stress, we find that treatment of animals with lupeol rescues some of the effects resulting from treatment with the prooxidant paraquat. Our results demonstrate that lupeol displays antioxidant properties in vivo in C. elegans .