Two-pore channel 1 interacts with citron kinase,regulating completion of cytokinesis

Two-pore channels (TPC1, 2, and 3) are recently identified endolysosmal ion channels, but remain poorly characterized. In this study, we show for the first time a role for TPC1 in cytokinesis, the final step in cell division. HEK 293 T-REx cells inducibly overexpressing TPC1 demonstrated a lack of proliferation accompanied by multinucleation and an increase in G2/M cycling cells. Increased TPC1 was associated with a concomitant accumulation of active RhoGTP and a decrease in phosphorylated myosin light chain (MLC). Finally, we demonstrated a novel interaction between TPC1 and citron kinase (CIT). These results identify TPC1 as a central component of cytokinetic control, specifically during abscission, and introduce a means by which the endolysosomal system may play an active role in this process.     

UTILIZATION OF PLANT MATERIALS BY JUVENILE AFRICAN CATFISH (CLARIAS GARIEPINUS) AND ITS IMPORTANCE IN FISH CULTURE

SUMMARY

Juvenile African catfish Clarias gariepinus between 100 and 200 mm total length from Lake McIlwaine, Zimbabwe are able to digest plant proteins. The digestibility of three major plant proteins (maize, sunflower seed and soya meal) was 30,0, 65,4 and 84,3% respectively. C. gariepinus excreted between 27 and 55% of its soluble nitrogen as urea. Fats from one diet were found to spare proteins and to be 73% utilized.

The basal metabolic rate of juvenile catfish may be represented by the general formula:

BM = 2,56 - 0,40 (In W) - 0,10 (In W) (FS)

where BM is the basal metabolic rate in cal g_?1 h_?1, W is the mass in grams and FS is the feeding state (expressed as zero for a feeding fish and one for a fasting fish).

The metabolism of starving, fasting, feeding, and stressed active juvenile fish was found to be approximately 0,28, 0,56, 1,23 and 4,5 cal. g_1 h_1 respectively.

World protein shortages and the contribution that fish culture can make are discussed. Sample calculations show catfish lose up to 38% of ingested plant protein while direct consumption of vegetative material by humans results in a loss of 33% of the protein due to imbalances in amino acid make-up of plants. It is generally not physically possible to eat the quantities of traditional low protein plant material needed to obtain the necessary protein. Therefore the use of more concentrated and more digestable animal protein is necessary, and catfish with dry weight ptotein levels of 70 to 80%, are capable of acting as protein concentrators.     

Nutrient transfer supports a beneficial relationship between the canopy ant,Azteca trigona,and its host tree

1. Energy fluxes between ants and plants have been a focal point for documenting mutualistic behaviour. Plants can provide resources to ants through the production of extrafloral nectaries. In exchange, ants can fertilise plants through their nutrient‐ and microbe‐rich refuse. 2. Here, we test a potential facultative mutualism between the carton‐nesting canopy ant, Azteca trigona, and their host trees. Through observational and experimental approaches, this study documents how nutrient transfer provides a basis for this beneficial ant–plant relationship. 3. In a greenhouse experiment, fertilisation with sterilised refuse (i.e. nutrients only) increased seedling growth three‐fold, while the refuse with its natural microbial community increased growth 11‐fold. 4. Total root density was doubled in refuse piles compared with the surrounding area in situ. On average, refuse provides host trees and the surrounding plant community with access to a > 800% increase in N, P and K relative to leaf litter. 5. Azteca trigona preferentially nests in trees with extrafloral nectaries and on large, longer‐lived tree species. 6. Given the nutrient‐poor nature of the Neotropics, host trees probably experience significant benefits from refuse fertilisation. Conversely, A. trigona benefit from long‐term stable structural support for nests and access to nutrient‐rich extrafloral nectaries. Without clear costs to either A. trigona or host trees, it is proposed that these positive interactions are preliminary evidence of a facultative mutualism.     

Association of cytochrome b5 with ETR1 ethylene receptor signaling through RTE1 in Arabidopsis

Ethylene plays important roles in plant growth, development and stress responses, and is perceived by a family of receptors that repress ethylene responses when ethylene is absent. Repression by the ethylene receptor ETR1 depends on an integral membrane protein, REVERSION TO ETHYLENE SENSITIVITY1 (RTE1), which acts upstream of ETR1 in the endoplasmic reticulum (ER) membrane and Golgi apparatus. To investigate RTE1 function, we screened for RTE1‐interacting proteins using the yeast split‐ubiquitin assay, which yielded the ER‐localized cytochrome b₅ (Cb5) isoform D. Cb5s are small hemoproteins that perform electron transfer reactions in all eukaryotes, but their roles in plants are relatively uncharacterized. Using bimolecular fluorescence complementation (BiFC), we found that all four ER‐localized Arabidopsis Cb5 isoforms (AtCb5–B, ‐C, ‐D and ‐E) interact with RTE1 in plant cells. In support of this interaction, atcb5 mutants exhibited phenotypic parallels with rte1 mutants in Arabidopsis. Phenotypes included partial suppression of etr1–2 ethylene insensitivity, and no suppression of RTE1‐independent ethylene receptor isoforms. The single loss‐of‐function mutants atcb5–b, ‐c and ‐d appeared similar to the wild‐type, but double mutant combinations displayed slight ethylene hypersensitivity. Over‐expression of AtCb5–D conferred reduced ethylene sensitivity similar to that conferred by RTE1 over‐expression, and genetic analyses suggested that AtCb5–D acts upstream of RTE1 in the ethylene response. These findings suggest an unexpected role for Cb5, in which Cb5 and RTE1 are functional partners in promoting ETR1‐mediated repression of ethylene signaling.