Conduct problems in childhood signal high future costs in terms of service utilization across multiple sectors. Future evaluations of interventions aimed at conduct problems should also track potential reductions in health burden and service usage that stretch into midlife.
Functions of isoamylase-type starch-debranching enzyme (ISA) proteins and complexes in maize (Zea mays) endosperm were characterized. Wild-type endosperm contained three high molecular mass ISA complexes resolved by gel permeation chromatography and native-polyacrylamide gel electrophoresis. Two complexes of approximately 400 kD contained both ISA1 and ISA2, and an approximately 300-kD complex contained ISA1 but not ISA2. Novel mutations of sugary1 (su1) and isa2, coding for ISA1 and ISA2, respectively, were used to develop one maize line with ISA1 homomer but lacking heteromeric ISA and a second line with one form of ISA1/ISA2 heteromer but no homomeric enzyme. The mutations were su1-P, which caused an amino acid substitution in ISA1, and isa2-339, which was caused by transposon insertion and conditioned loss of ISA2. In agreement with the protein compositions, all three ISA complexes were missing in an ISA1-null line, whereas only the two higher molecular mass forms were absent in the ISA2-null line. Both su1-P and isa2-339 conditioned near-normal starch characteristics, in contrast to ISA-null lines, indicating that either homomeric or heteromeric ISA is competent for starch biosynthesis. The homomer-only line had smaller, more numerous granules. Thus, a function of heteromeric ISA not compensated for by homomeric enzyme affects granule initiation or growth, which may explain evolutionary selection for ISA2. ISA1 was required for the accumulation of ISA2, which is regulated posttranscriptionally. Quantitative polymerase chain reaction showed that the ISA1 transcript level was elevated in tissues where starch is synthesized and low during starch degradation, whereas ISA2 transcript was relatively abundant during periods of either starch biosynthesis or catabolism.Starch biosynthesis is a central function in plant metabolism that is accomplished by a multiplicity of conserved enzymatic activities. Two known activities are starch synthase, which catalyzes the polymerization of glucosyl units into a(1/4)-linked "linear" chains, and starch-branching enzyme, which catalyzes the formation of a(1/6) glycoside bond branches that join linear chains. Acting together, the starch synthases and starch-branching enzymes assemble the relatively highly branched polymer amylopectin, with approximately 5% of the glucosyl residues participating in a (1/6) bonds, and the lightly branched molecule amylose. Amylopectin and amylose assemble into semicrystalline starch granules, which in land plants and green algae are located in plastids.A third activity necessary for normal starch biosynthesis is provided by starch-debranching enzyme (DBE), which hydrolyzes a(1/6) linkages. Two DBE classes have been conserved separately in plants (Beatty et al., 1999). These are referred to here as pullulanase-type DBE (PUL) and isoamylase-type DBE (ISA), based on similarity to prokaryotic enzymes with particular substrate specificity. ISA function in starch production is implied from genetic observations that mutations typically result in reduced ...
This study characterized genetic interactions between the maize (Zea mays) genes dull1 (du1), encoding starch synthase III (SSIII), and isa2, encoding a noncatalytic subunit of heteromeric isoamylase-type starch-debranching enzyme (ISA1/ISA2 heteromer). Mutants lacking ISA2 still possess the ISA1 homomeric enzyme. Eight du1 -mutations were characterized, and structural changes in amylopectin resulting from each were measured. In every instance, the same complex pattern of alterations in discontinuous spans of chain lengths was observed, which cannot be explained solely by a discrete range of substrates preferred by SSIII. Homozygous double mutants were constructed containing the null mutation isa2-339 and either du1-Ref, encoding a truncated SSIII protein lacking the catalytic domain, or the null allele du1-R4059. In contrast to the single mutant parents, double mutant endosperms affected in both SSIII and ISA2 were starch deficient and accumulated phytoglycogen. This phenotype was previously observed only in maize sugary1 mutants impaired for the catalytic subunit ISA1. ISA1 homomeric enzyme complexes assembled in both double mutants and were enzymatically active in vitro. Thus, SSIII is required for normal starch crystallization and the prevention of phytoglycogen accumulation when the only isoamylase-type debranching activity present is ISA1 homomer, but not in the wild-type condition, when both ISA1 homomer and ISA1/ISA2 heteromer are present. Previous genetic and biochemical analyses showed that SSIII also is required for normal glucan accumulation when the only isoamylase-type debranching enzyme activity present is ISA1/ISA heteromer. These data indicate that isoamylase-type debranching enzyme and SSIII work in a coordinated fashion to repress phytoglycogen accumulation.Semicrystalline glucan polymers that form insoluble starch granules are found in the vast majority of organisms within the Archaeplastida lineage of primary photosynthetic eukaryotes. This group, which comprises glaucophytes, rhodophytes (red algae), and Chloroplastida (green algae and land plants), in general does not contain soluble glucan polymers of substantial size. Conversely, with a few exceptions, essentially all other eukaryotes and prokaryotes utilize the soluble polymer glycogen for the storage of Glc and lack any insoluble glucans. Starch granules and their constituent polymers are capable of storing many more Glc units than chemically similar but soluble glucans, and this is likely to have provided a selective advantage during the establishment and spread of the photosynthetic eukaryotes. Support for this suggestion comes from the facts that the primary photosynthetic eukaryotes are a monophyletic group (Rodríguez-Ezpeleta et al., 2005). In light of the important role of starch metabolism in these organisms, including the land plants, it is of interest to understand the molecular mechanisms that generate semicrystalline glucans and how these processes differ from those that generate glycogen.Starch granules are made up of two t...
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