Increased expression of p62 in expanded polyglutamine-expressing cells and its association with polyglutamine inclusions

Huntington's disease is a progressive neurodegenerative disorder that is associated with a CAG repeat expansion in the gene encoding huntingtin. We found that a 60-kDa protein was increased in Neuro2a cells expressing the N-terminal portion of huntingtin with expanded polyglutamine. We purified this protein, and, using mass spectrometry, identified it as p62, an ubiquitin-associated domain-containing protein. A specific p62 antibody stained the ubiquitylated polyQ inclusions in expanded polyglutamine-expressing cells, as well as in the brain of the huntingtin exon 1 transgenic mice. Furthermore, the level of p62 protein and mRNA was increased in expanded polyglutamine-expressing cells. We also found that p62 formed aggresome-like inclusions when p62 was increased in normal Neuro2a cells by a proteasome inhibitor. Knock-down of p62 does not affect the formation of aggresomes or polyglutamine inclusions, suggesting that p62 is recruited to the aggresome or inclusions secondary to their formation. These results suggest that p62 may play important roles as a responsive protein to a polyglutamine-induced stress rather than as a cross-linker between ubiquitylated proteins.     

Identification of rice Allene Oxide Cyclase mutants and the function of jasmonate for defence against Magnaporthe oryzae

Two photomorphogenic mutants of rice, coleoptile photomorphogenesis 2 (cpm2) and hebiba, were found to be defective in the gene encoding allene oxide cyclase (OsAOC) by map‐based cloning and complementation assays. Examination of the enzymatic activity of recombinant GST–OsAOC indicated that OsAOC is a functional enzyme that is involved in the biosynthesis of jasmonic acid and related compounds. The level of jasmonate was extremely low in both mutants, in agreement with the fact that rice has only one gene encoding allene oxide cyclase. Several flower‐related mutant phenotypes were observed, including morphological abnormalities of the flower and early flowering. We used these mutants to investigate the function of jasmonate in the defence response to the blast fungus Magnaporthe oryzae. Inoculation assays with fungal spores revealed that both mutants are more susceptible than wild‐type to an incompatible strain of M. oryzae, in such a way that hyphal growth was enhanced in mutant tissues. The level of jasmonate isoleucine, a bioactive form of jasmonate, increased in response to blast infection. Furthermore, blast‐induced accumulation of phytoalexins, especially that of the flavonoid sakuranetin, was found to be severely impaired in cpm2 and hebiba. Together, the present study demonstrates that, in rice, jasmonate mediates the defence response against blast fungus.     

The aphid Ceratovacuna nekoashi (Hemiptera: Aphididae: Hormaphidinae) and its allied species in Korea,Japan and Taiwan

The aphid Ceratovacuna nekoashi and its allied species have been a taxonomically difficult group. They form peculiar “cat's‐paw” galls (called “Nekoashi” in Japanese) on Styrax trees and also use Microstegium grasses as their secondary hosts. Through sampling aphids from both Styrax galls and Microstegium grasses in South Korea, Japan and Taiwan, and sequencing their DNA, we made it clear that four distinct species occur in these regions: C. nekoashi (Sasaki), C. oplismeni (Takahashi), C. orientalis (Takahashi) and C. subtropicana sp. nov. In Korea, C. nekoashi forms galls on both S. japonicus and S. obassia, whereas in Japan the species forms galls on the former but not on the latter; our molecular analyses unequivocally indicated the occurrence of a single species in South Korea and mainland Japan. Aphids of the four species on the secondary host were morphologically discriminated from one another. The identity of the primary‐ and secondary‐host generations was also clarified for each species. All four species were found to produce second‐instar sterile soldiers in their Styrax galls, and first‐instar soldiers were found in colonies of C. subtropicana on the secondary host.     

Genetic interactions involved in the inhibition of heading by heading date QTL, <Emphasis Type="Italic">Hd2</Emphasis> in rice under long-day conditions

Heading date is the one of the most important traits in rice breeding, because it defines where rice can be cultivated and influences the expression of various agronomic traits. To examine the inhibition of heading by Heading date 2 (Hd2), previously detected on the distal end of chromosome 7’s long arm by quantitative trait locus (QTL) analysis, we developed backcross inbred lines (BILs) from Koshihikari, a leading Japanese cultivar, and Hayamasari, an extremely early heading cultivar. The BILs were cultivated under natural field conditions in Tsukuba Japan, and under long-day (14.5 h), extremely long-day (18 h), and short-day (10 h) conditions. Combinations of several QTLs near Hd1, Hd2, Ghd7, Hd5, and Hd16 were detected under these four conditions. Analysis of advanced backcross progenies revealed genetic interactions between Hd2 and Hd16 and between Hd2 and Ghd7. In the homozygous Koshihikari genetic background at Hd16, inhibition of heading by the Koshihikari allele at Hd2 was smaller than that with the Hayamasari Hd16 allele. Similarly, in the homozygous Koshihikari genetic background at Ghd7, the difference in heading date caused by different alleles at Hd2 was smaller than in plants homozygous for the Hayamasari Ghd7 allele. Based on these results, we conclude that Hd2 and its genetic interactions play an important role in controlling heading under long-day conditions. In addition, QTLs near Hd2, Hd16, and Ghd7, which are involved in inhibition of heading under long-day conditions, function in the same pathway that controls heading date.     

Expression of the Pib rice-blast-resistance gene family is up-regulated by environmental conditions favouring infection and by chemical signals that trigger secondary plant defences

The rice blast resistance gene Pib is a member of the nucleotide binding site (NBS) and leucine-rich repeat (LRR) class of plant disease resistance (R) genes and belongs to a small gene family. We describe here the isolation and characterization of a Pib homologue (PibH8), and extensive investigation of the expression of the Pib gene family (Pib, PibH8, HPibH8-1, HPibH8-2) under various environmental and chemical treatments. PibH8 shows 42% identity and 60% similarity to Pib and, like Pib, has a duplication of the kinase 1a, 2, and 3a motifs of the NBS region in the N-terminal half of the protein. Interestingly, genes of the Pib family exhibit a diurnal rhythm of expression. RNA gel blot analysis revealed that their expression was regulated dramatically by environmental signals. such as temperature, light and water availability. Their expression was also induced by chemical treatments, such as jasmonic acid, salicylic acid, ethylene and probenazole. Our findings suggest that expression of the Pib gene family is up-regulated by environmental conditions that would favour pathogen infection. This may reflect the evolution of anticipatory control of R gene expression.     

Two closely related species of Nipponaphis (Hemiptera: Aphididae) that migrate between Distylium racemosum and Machilus trees in Japan

Nipponaphis loochooensis Sorin, 1996 and N. machilicola (Shinji, 1941) form fig‐shaped or globular galls on Distylium racemosum in southern Japan. Nipponaphis machilicola migrates to the lauraceous evergreen Machilus thunbergii. Nipponaphis loochooensis has also been supposed to migrate to M. thunbergii, but its secondary‐host generation has not been found in the field to date. Through sampling Nipponaphis aphids from trees of M. japonica in addition to M. thunbergii, and sequencing their mitochondrial DNA, we found that the two species form colonies on twigs of both Machilus species, and that the two at times colonize on the same trees and even form mixed colonies. Only N. loochooensis forms colonies on leaves of M. japonica, but neither species colonizes on leaves of M. thunbergii. The secondary‐host generations of the two species could be clearly discriminated from each other, based on morphology. It was confirmed by examining the type specimens of Nipponaphis amamiana Takahashi, 1962 that the name is a junior synonym of N. machilicola.