Inhibition of the formation of adventitious roots on cucumber hypocotyls by the fractions and methoxybenzylglutamine from xylem sap of squash root

In studies of the functions of roots in the development of aboveground organs, the butanol fraction of xylem sap collected from squash root was found to have inhibitory activity against the formation of adventitious roots on the hypocotyls of cucumber in a culture of shoot cutting. The inhibitory activity was fractionated with reverse phase column chromatographies, and an inhibitory fraction was recovered with a single peak of absorbance at 280 nm, which contained a novel amino acid,N ⁵-(4-methoxyphenyl) methyl-l-glutamine (methoxybenzylglutamine) as a major component (Inouyeet al. 1998). Chemically synthesized methoxybenzylglutamine (5 mM) inhibited the formation of adventitious roots and also inhibited the growth of first leaf and cotyledons in a culture of shoot cuttings. On the basis of the results obtained, discussed is possible regulation of the developmental events on the aboveground organs by the roots through xylem sap.     

Enrichment and efficient screening of ES cells containing a targeted mutation: the use of DT‐A gene with the polyadenylation signal as a negative selection maker

Gene targeting in embryonic stem (ES) cells via homologous recombination can occur at very low frequency. In order to enrich homologous recombinants before screening, a negative selection marker, such as thymidine kinase (TK) and diphtheria toxin A fragment (DTA), has been commonly used. In this study, we developed a negative selection marker using DTA gene with polyadenylation signal and it was designated DTApA. To determine the difference in targeting efficiency of the negative selections, we constructed three different targeting vectors for each negative selection (first, TK at the 3 end, second, TK at both the 5 and 3 ends <2 X TK>, and third, DTApA at the 5 end of the homologous sequences). Gene targeting experiments using these constructs clearly showed that negative selection using DTApA was more efficient than that using TK for homologous recombination and that negative selection using DTApA was as efficient as that using 2 X TK. Considering the fact that the use of DTApA is more convenient for construction of targeting vectors than that of 2 X TK, DTApA is an efficient negative selection marker.In addition, we examined long and accurate PCR (LAPCR) for screening gene targeted clones. The use of LAPCR with genomic DNAs from ES cell clones facilitated simple detection of homologous recombinants, suggesting that the screening with LAPCR is compatible with the use of longer homologous sequences of both arms in vector design. Our results indicate that the use of DTApA for negative selection together with the application of LAPCR for screening ensures efficient and timesaving screening for homologous recombinants.     

Escherichia coli small heat shock proteins, IbpA and IbpB, protect enzymes from inactivation by heat and oxidants.

To examine functions of two small heat shock proteins of Escherichia coli, IbpA and IbpB, we constructed His-IbpA and His-IbpB, in which a polyhistidine tag was fused to the N-terminals. Both purified His-IbpA and His-IbpB formed multimers, which have molecular masses of about 2.0-3.0 MDa and consist of about 100-150 subunits. They suppressed the inactivation of several enzymes including citrate synthase and 6-phosphogluconate dehydrogenase by heat, potassium superoxide, hydrogen peroxide and freeze-thawing, but not the inactivation of glyceraldehyde-3-phosphate dehydrogenase by hydrogen peroxide. Both His-IbpA and His-IbpB suppressed enzyme inactivation by various treatments and were also found to be associated with their non-native forms. However, both His-IbpA and His-IbpB were not able to reactivate enzymes inactivated by heat, oxidants or guanidine hydrochloride. When heated to 50 degrees C, each multimeric form of His-IbpA or His-IbpB was dissociated to form a monomer for His-IbpA, and an oligomer of about one-quarter size for His-IbpB. These structural changes were reversible, as both heated proteins regained the multimeric structures after incubation at 25 degrees C. However, when exposed to hydrogen peroxide or potassium superoxide, the large multimeric forms of His-IbpA and His-IbpB were maintained. The results suggest that His-IbpA and His-IbpB suppress the inactivation of enzymes and bind non-native proteins to protect their structures from heat and oxidants.     

Mosaic formation by developmental loss of a chromosomal fragment in a “mottled striped” mosaic strain of the silkworm,Bombyx mori

A separable chromosomal fragment of about 2.5 Mb, which carries the larval body marking gene striped (p ^S), is present in a recessive background in the kind of genetic mosaic called mottled striped in the silkworm, Bombyx mori. The somatic loss of this chromosomal fragment during cell division gives rise to white patches (variegated pigmentation) in the dorsal black stripes of the fifth instar larva. Each larger white patch in the black p ^S stripe represents the clonal expansion of an epidermal cell that lost the fragment carrying p ^S during an early developmental stage. To gain information on the developmental history of the larval epidermal cells, we have analysed a variety of mosaic individuals showing extreme mottling patterns. Based on several common features observed in mosaic patterns, we constructed a schematic model for migration of epidermal cells, which implies that several polyclonal founding cells on each lateral side of a segment move and expand toward the dorsal mid-line. To determine the timing of loss of the fragment in half-stripe mosaics, which are completely lacking the mottled black stripe on one half of the larval body, we examined several tissues from either body side for the chromosomal fragment. Pulsed field gel electrophoresis (PFGE) and restriction fragment length polymorphism (RFLP) analysis showed that testes and silk glands from each side of the half-stripe mosaics (two and five individuals, respectively) contained the chromosomal fragment carrying the p ^S allele, independent of the epidermal phenotypes of the respective body half. This result suggests that loss of the chromosomal fragment leading to external half-stripe mosaics might occur, not at an early stage of development such as the first nuclear division, but rather after the progenies of epidermis and internal tissues examined here diverged from each other developmentally.