Hao H et al. (2019) Nucleus "SUN/KASH interactions facilitate force transmission across the nuclear envelope."

Starr DA, Hao H

[Nucleus, 2019]

LINC complexes (Linker of Nucleoskeleton and Cytoskeleton), consisting of inner nuclear membrane SUN proteins and outer nuclear membrane KASH proteins, are essential for nuclear positioning, cell migration and chromosome dynamics. Crystal structures of the central SUN-KASH interaction domains revealed close interfaces predicted to mediate LINC complex formation and function. However, the in vivo significance of these conserved interactions were unclear. Cain et al (2018) used a combination of Caenorhabditis elegans genetics, imaging in cultured NIH 3T3 fibroblasts, and Molecular Dynamic simulations, to study SUN-KASH interactions in cells. The study found that a conserved aromatic residue at the -7 position of the C-terminal KASH domain and conserved cysteines in both the KASH and SUN domains play important roles in force transmission across the nuclear envelope. Other properties of LINC complexes may also play significant roles in transmitting mechanical forces generated by the cytoskeleton across the nuclear envelope. For example, the helicies preceding the SUN domain activate SUN proteins and may be important for activating KASH-SUN interactions or for association of SUN and/or KASH proteins with the membrane. The longer coiled-coils spanning the perinuclear space may also play a role in mediating force transmission. Finally, LINC complexes may be arranged in higher-order structures to facilitate high force-bearing processes.

Thomas JH et al. (1994) Worm Breeder's Gazette "lin-36, a Class B Synthetic Multivulva Gene, Encodes a Novel Protein"

Thomas JH, Horvitz HR

[Worm Breeder's Gazette, 1994]

lin-36, a Class B Synthetic Multivulva Gene, Encodes a Novel Protein Jeffrey H. Thomas and H. Robert Horvitz, HHMI, Dept. Biology, MIT, Cambridge, MA 02139, USA

Sun J et al. (2013) Exp Parasitol "Parasitism of secondary-stage juvenile of Heterodera glycines and four larva stages of Caenorhabditis elegans by Hirsutella spp."

Sun J, Xie H, Xiang M, Liu X, Qiu J

[Exp Parasitol, 2013]

The fungi Hirsutella rhossiliensis and Hirsutella minnesotensis generally parasitize only plant-parasitic nematodes in nature but parasitize the bacterivorous nematode Caenorhabditis elegans on agar plates. To establish a model system for studying the interaction between fungi and nematodes, we compared the parasitism of the first- to fourth-stage larvae (L1-L4) of C. elegans and second-stage juvenile (J2) of Heterodera glycines by twenty isolates of Hirsutella spp. Although parasitism differed substantially among isolates, both H. minnesotensis and H. rhossiliensis parasitized a higher percentage of H. glycines J2s than of C. elegans larvae. Parasitism of C. elegans L1s was correlated with parasitism of H. glycines J2s. Parasitism of C. elegans by H. rhossiliensis and H. minnesotensis was negatively correlated with larva size and motility, i.e., parasitism was higher for the younger stages. The C. elegans L1 is recommended for studying parasitism of nematodes by H. rhossiliensis and H. minnesotensis.

Fei YJ et al. (2000) J Biol Chem "A novel H(+)-coupled oligopeptide transporter (OPT3) from Caenorhabditis elegans with a predominant function as a H(+) channel and an exclusive expression in neurons."

Leibach FH, Romero MF, Krause MW, Huang W, Ganapathy V, Fei YJ, Liu JC

[J Biol Chem, 2000]

We have cloned and functionally characterized a novel, neuron-specific, H(+)-coupled oligopeptide transporter (OPT3) from Caenorhabditis elegans that functions predominantly as a H(+) channel. The opt3 gene is approximately 4.4 kilobases long and consists of 13 exons. The cDNA codes for a protein of 701 amino acids with 11 putative transmembrane domains. When expressed in mammalian cells and in Xenopus laevis oocytes, OPT3 cDNA induces H(+)-coupled transport of the dipeptide glycylsarcosine. Electrophysiological studies of the transport function of OPT3 in Xenopus oocytes show that this transporter, although capable of mediating H(+)-coupled peptide transport, functions predominantly as a H(+) channel. The H(+) channel activity of OPT3 is approximately 3-4-fold greater than the H(+)/peptide cotransport activity as determined by measurements of H(+) gradient-induced inward currents in the absence and presence of the dipeptide using the two-microelectrode voltage clamp technique. A downhill influx of H(+) was accompanied by a large intracellular acidification as evidenced from the changes in intracellular pH using an ion-selective microelectrode. The H(+) channel activity exhibits a K(0.5)(H) of 1.0 microM at a membrane potential of -50 mV. At the level of primary structure, OPT3 has moderate homology with OPT1 and OPT2, two other H(+)-coupled oligopeptide transporters previously cloned from C. elegans. Expression studies using the opt3::gfp fusion constructs in transgenic C. elegans demonstrate that opt3 gene is exclusively expressed in neurons. OPT3 may play an important physiological role as a pH balancer in the maintenance of H(+) homeostasis in C. elegans.

Imadzu H et al. (1994) Worm Breeder's Gazette "Two Tropomyosins Expressed in Body Wall and the Third Did In Pharynx of Caenorhabditis elegans"

Kagawa H, Sakube Y, Imadzu H

[Worm Breeder's Gazette, 1994]

TWO TROPOMYOSINS EXPRBSSBD IN BODY WALL AND THE THIRD DID IN PHARYNX OF CAENORHABDDITIS ELEGANS. H. Imadzu, Y. Sakube and H. gagawa. Department of Biology, Faculty of Science, Okayama University, Okayama, 700 Japan.

Wilson PA et al. (1982) Parasitology "Strongyloides ratti (homogonic): the time-course of early migration in the generalized host deduced from experiments in lactating rats."

Steven GE, Simpson NE, Wilson PA

[Parasitology, 1982]

Unsuckled mother rats given a 1 h suckling stimulus 3 h after subcutaneous injection of an exact dose of homogonic Strongyloides ratti allow fewer worms to develop in their intestines by day 9 than nulliparous rats (Wilson & Simpson, 1981). This effect is studied in more detail in terms of the length of time between weaning and stimulus (W leads to S) and injection and stimulus (I leads to S). It was observable with a W leads to S of 30 h but this and a period of 5 h were less effective than 24 h. With W leads to S constant at 24 h, significantly more worms developed in mothers when I leads to S was 24 h compared to 3 h and 10 h (P less than 0.005). The data, combined with those from nulliparous controls, are presented as a measure of the change with time of numbers of larvae in that compartment of the system which gives access to the stimulated mammary gland. It is argued that the particular compartment is the local lymph node draining the injection site and that the kinetics deduced are applicable to migration in the rat in general.

Miller DL et al. (2007) Proc Natl Acad Sci U S A "Hydrogen sulfide increases thermotolerance and lifespan in Caenorhabditis elegans."

Miller DL, Roth MB

[Proc Natl Acad Sci U S A, 2007]

Hydrogen sulfide (H(2)S) is naturally produced in animal cells. Exogenous H(2)S has been shown to effect physiological changes that improve the capacity of mammals to survive in otherwise lethal conditions. However, the mechanisms required for such alterations are unknown. We investigated the physiological response of Caenorhabditis elegans to H(2)S to elucidate the molecular mechanisms of H(2)S action. Here we show that nematodes exposed to H(2)S are apparently healthy and do not exhibit phenotypes consistent with metabolic inhibition. Instead, animals exposed to H(2)S are thermotolerant and long-lived. These phenotypes require SIR-2.1 activity but are genetically independent of the insulin signaling pathway, mitochondrial dysfunction, and caloric restriction. These studies suggest that SIR-2.1 activity may translate environmental change into physiological alterations that improve survival. It is interesting to consider the possibility that the mechanisms by which H(2)S increases thermotolerance and lifespan in nematodes are conserved and that studies using C. elegans may help explain the beneficial effects observed in mammals exposed to H(2)S.

Cain, N. et al. (2017) International Worm Meeting "Interactions between SUN and KASH proteins in vivo during nuclear migration, nuclear anchorage, and the developmental switch between moving and stationary nuclei."

Cain, N., Starr, D.A., Hao, H.

[International Worm Meeting, 2017]

LINC complexes, consisting of SUN proteins in the inner nuclear membrane and KASH proteins in the outer nuclear membrane, transfer forces between the cytoskeleton and the nucleoskeleton. One role of LINC complexes is to mediate nuclear positioning. The canonical C. elegans SUN protein UNC-84 interacts with two different KASH proteins-UNC-83 (a functional homolog of mammalian Nesprin-4 and KASH5) to move nuclei via microtubule motors and ANC-1 (the ortholog of the giant mammalian Nesprin-1 and -2) to anchor nuclei to actin. It is not known how UNC-84 chooses between binding UNC-83 to move nuclei or binding ANC-1 to anchor nuclei. Based on structural data of human SUN-KASH complexes, we first hypothesized that key conserved residues in the SUN domain of UNC-84 are required to interact with the C-termini of KASH proteins. Both UNC-84(S1034E) and UNC-84(C994E) failed to recruit UNC-83 to the nuclear envelope and nuclear migration was blocked. Second, the structure predicted that the length of the C-terminus of KASH proteins is limited by the size of the binding pocket in the SUN domain. The addition of a single alanine to the end of UNC-83 completely blocked UNC-83 localization and nuclear migration in vivo. Finally, the structure identified an intermolecular di-sulfide bond between conserved cysteine residues in SUN and KASH proteins. The conserved cysteine at position -23 of KASH proteins is present in ANC-1, but not in UNC-83. This led us to hypothesize that cysteine bonds are dispensable for nuclear migration, but required for nuclear anchorage. To test this hypothesis, we used CRISPR/Cas9-mediated genome editing to mutate conserved cysteines in SUN and KASH proteins. Hypodermal nuclei expressing UNC-84(C953A) migrated normally, but clustered unevenly in the adult syncytium. Similar anchorage defects in the adult animal were observed after mutating the conserved cysteine in the KASH domain of ANC-1, or replacing the KASH domain of ANC-1 with the KASH domain of UNC-83, which does not have a cysteine. Based on these results, our model is that di-sulfide bonds between SUN proteins and various KASH partners could be a component of a molecular switch between actively moving and anchored nuclei. Interestingly, careful quantification of the nuclear anchorage phenotype shows that unc-84 mutants are not as severe as anc-1 mutants, suggesting ANC-1 has activities independent of UNC-84. We are currently testing potential ANC-1 partners to see if they enhance nuclear anchorage defects of unc-84.

Sakube Y et al. (1994) Worm Breeder's Gazette "The Genome Structure and Expression of Promoter/lacZ Fusion Genes of C. elegans Ryanodine Receptor"

Imadzu H, Sakube Y, Kagawa H

[Worm Breeder's Gazette, 1994]

The Genome Structure and Expression of Promoter/lacZ Fusion Genes of the C. elegans Ryanodine Receptor Y. Sakube, H. Imadzu and H. Kagawa, Laboratory of Molecular Biology, Faculty of Science, Okayama University, Okayama, 700 Japan C51918@JPNKUDPC

Valles P et al. (2006) Semin Nephrol "Kidney vacuolar H+ -ATPase: physiology and regulation."

Wysocki J, Batlle D, Lapointe MS, Valles P

[Semin Nephrol, 2006]

The vacuolar H(+)-ATPase is a multisubunit protein consisting of a peripheral catalytic domain (V(1)) that binds and hydrolyzes adenosine triphosphate (ATP) and provides energy to pump H(+) through the transmembrane domain (V(0)) against a large gradient. This proton-translocating vacuolar H(+)-ATPase is present in both intracellular compartments and the plasma membrane of eukaryotic cells. Mutations in genes encoding kidney intercalated cell-specific V(0) a4 and V(1) B1 subunits of the vacuolar H(+)-ATPase cause the syndrome of distal tubular renal acidosis. This review focuses on the function, regulation, and the role of vacuolar H(+)-ATPases in renal physiology. The localization of vacuolar H(+)-ATPases in the kidney, and their role in intracellular pH (pHi) regulation, transepithelial proton transport, and acid-base homeostasis are discussed.