The yeast Hex3.Slx8 heterodimer is a ubiquitin ligase stimulated by substrate sumoylation

Hex3 and Slx8 are Saccharomyces cerevisiae proteins with important functions in DNA damage control and maintenance of genomic stability. Both proteins have RING domains at their C termini. Such domains are common in ubiquitin and ubiquitin-like protein ligases (E3s), but little was known about the molecular functions of either protein. In this study we identified HEX3 as a high-copy suppressor of a temperature-sensitive small ubiquitin-related modifier (SUMO) protease mutant, ulp1ts, suggesting that it may affect cellular SUMO dynamics. Remarkably, even a complete deletion of ULP1 is strongly suppressed. Hex3 forms a heterodimer with Slx8. We found that the Hex3.Slx8 complex has a robust substrate-specific E3 ubiquitin ligase activity. In this E3 complex, Slx8 appears to bear the core ligase function, with Hex3 strongly enhancing its activity. Notably, SUMO attachment to a substrate stimulates its Hex3.Slx8-dependent ubiquitination, primarily through direct noncovalent interactions between SUMO and Hex3. Our data reveal a novel mechanism of substrate targeting in which sumoylation of a protein can help trigger its subsequent ubiquitination by recruiting a SUMO-binding ubiquitin ligase.     

Intergeneric Hybridisation between Litchi (Litchi chinensis Sonn.) and Longan (Dimocarpus longan Lour.)

The breeding barriers between commercial litchi (Litchi chinensisSonn.) and longan (Dimocarpus longan Lour.) cultivars were investigatedby conducting reciprocal pollinations. This work has shown thatit is possible to generate intergeneric hybrids using litchias the female parent. Investigation of comparative in vivo pollentube growth demonstrated that there is discrimination againstcross- compared to self-pollen at all sites in the pistil. Pollentubes were frequently observed in the ovary after cross-pollinationin litchi but rarely in longan. Fruit production was reducedafter crossing in both longan and litchi. Isozyme analysis usingphosphoglucose isomerase revealed that hybrid progeny only developedwhen litchi was the maternal parent. Morphologically the hybridplants were similar to the maternal parent but leaves were smaller.Three types of seeds developed in litchi following pollinationwith longan pollen. These were (1) normal seeds with a developedtesta and embryo, (2) seeds with aborted embryos but normaltesta development, and (3) seedless fruit where the ovule remainedthe same size as at anthesis without further development ofembryo or testa. The potential germplasm available to improvethese crops within the Sapindaceae is discussed.Copyright 1994,1999 Academic Press Litchi, Litchi Longan, Dimocarpus, hybridisation, isozyme     

Reproduction in seagrasses: pollen wall morphogenesis in Amphibolis antarctica and wall structure in filiform grains

The pre–meiotic anther of the marine angiosperm Amphibolis antarctica contains microsporocytes and sterile cells. The microsporocytes divide conventionally to produce tetrads, but the sterile cells degenerate and contribute to the future pe–riplasmodium. Each tetrad of young microspores is contained within a vesicle defined by a membrane. After release from the tetrad, the microspores increase in length and rapidly become filiform. The microspore nucleus soon divides and partitioning of the cytoplasm delimits the generative cell from the vegetative cell of the binucleate pollen grain. The division and the early pollen growth occurs while the grains are segregated within vesicles in the periplasmodium. These compartments, established at microspore release, remain structurally intact throughout the vacuolate period of pollen development, when pollen wall assembly begins. This process is initiated as particles migrate from the inner face of the vesicle membrane into the lumen of the vesicle and microfibrillar elements form between adjacent particles. The particles and microfibrils form a loose, three–dimensional network. The vesicle membrane then disappears and the binuclate grains become immersed in the tapetal residuum. Additional wall components are now deposited upon the primary fibrillar stratum. Short lamellae, resembling fragments of membrane, frequently associated with electron–opaque globuli, are found intermixed with the surface microfibrils. Apparently, granular material originating in the degenerating periplasmodium may be the precursor of the globuli, and contact with the lamellae brings about an alteration in state. At this stage the pollen wall is resolved as two distinct fibrillar strata and the lamellae and globuli are incorporated as inclusions into the superficial zone of the outer stratum. The mature pollen wall exhibits faint stratification and the presence of the subsurface inclusions is readily demonstrated in germinating grains by section staining with phosphotungstic acid. The pollen wall in A. antarctica is compared with that in filiform grains of other seagrasses.     

Molecular heterogeneity in McArdle's disease

Biopsies were taken from a group of eleven patients with McArdle's disease, a congenital deficiency in muscle glycogen phosphorylase. The biopsies were screened by Western and Northern blotting for phosphorylase protein, phosphotrylase-bound pyridoxal-5′-phosphate (the cofactor of the enzyme) and for phosphorylase mRNA. Of the eleven patients, three expressed phosphorylase mRNA at near normal levels and at the expected size. One of these patients also expressed low levels of phosphorylase protein that correlated with a small amount of measurable phosphorylase activity. These data support the contention of molecular heterogeneity in the presentation of this phenotype.