An electrophoretic polymorphism in salivary amylases (Amy-1) of mastomys (Praomys coucha).

An electrophoretic polymorphism of salivary amylases (Amy-1) in mastomys (Praomys coucha) (MWC, MRJ and MCC strains) was detected. Amylase in MWC or MRJ saliva, which migrated fast toward the anode, was designated as AMY-1A, and that in MCC saliva migrating slowly as AMY-1B. Salivary amylases are controlled by a pair of codominant alleles at a single autosomal locus (Amy-1). No polymorphism was seen in pancreatic amylases (Amy-2). The frequencies of these phenotypes did not differ between the sexes. Some isoamylases were observed and these were different from those in mouse or rat.     

Genetic variants found in plasma alpha-amylase and erythrocyte carbonic anhydrase in the musk shrew (Suncus murinus)

Genetic variants of plasma alpha-amylase and erythrocyte carbonic anhydrase in the musk shrew (Suncus murinus) were found by electrophoreses using cellulose acetate plates. It was demonstrated that phenotypic differences of alpha-amylase are controlled by two codominant alleles (Amy-1a and Amy-1b) at a single autosomal locus (Amy-1). The segregation data of the carbonic anhydrase phenotypes in the progeny supported the genetic theory of two codominant alleles (Car-1a and Car-1b) at a single autosomal locus (Car-1). The data suggested that there was no close linkage between the two loci, Amy-1 and Car-1. The Car-1 locus was fixed with one of the two alleles in each of the four lines, i.e. Nag, Oki , Tar and Jak originating from wild animals captured in Nagasaki and Naha and Tarama Island, Okinawa, Japan, and in Jakarta, Indonesia, respectively. Oki and Tar lines still showed segregation of the two alleles at the Amy-1 locus.     

Salivary gland amylase polymorphism in pigs and cattle detected by affinity electrophoresis

New allelic variants of salivary gland alpha-amylase in pigs (AMY-1C, AMY-1D) have been detected using affinity electrophoresis. In yak, zebu and in hybrids (yak x cattle, zebu x cattle) a new AMY-1 allelic variant (AMY-1D) has been found using the same method.     

Expression of genes controlling modification of amylase in hybrids and original representatives of a cattle subfamily (Bovinae)]

Modifications of similar type were noted in the number of multiple AMY-1 forms of amylase isozyme for various species of Artiodactyla. It is supposed that these modifications are linked to periodical activation during evolution of genes responsible for modification of the molecules. Data obtained on Bovinae hybrids testify to this point of view. Inactivation of active and reinactivation of "silent" genes responsible for modification of AMY-1 molecules are observed in hybrids of bison x cow and bison x aurochs combinations.     

近年来华东地区家鸭中禽流感病毒的亚型分布

[目的]为了研究近年来华东地区家鸭中禽流感病毒的亚型分布情况.[方法]对2002-2006年分离自华东地区家鸭的180株禽流感病毒的HA亚型和其中88株禽流感病毒的NA亚型分别进行了测定.[结果]近年来华东地区家鸭中至少存在9种HA亚型和6种NA亚型组成的H1N1,H3N1,H3N2,H3N8,H4N6,H5N1,H5N2,H6N2,H6N8,H8N4,H9N2,H10N3,H11N2共13种亚型的禽流感病毒.[结论]华东地区家鸭中有多种亚型的禽流感病毒分布,应加强家鸭禽流感的监测和防制工作.     

Alleles at plasma alpha-amylase locus(Amy-1) of the house musk shrew(Suncus murinus): frequency distribution and new variants in laboratory lines and local Asian populations

Among nine laboratory shrew lines originating from the Japanese islands (Nag, Tok, TKU, Ize, Tr and OKI lines), West Java (Bog), Bangladesh (BAN) and Sri Lanka (SRI), Nag, Tr and Bog were fixed with Amy-1b and SRI with Amy-1a. The remaining lines were still highly polymorphic with the two alleles. A new electrophoretic band C was found in the BAN line and concluded to be expressed by a codominant allele, Amy-1c, which was carried by a single heterozygous female from among eleven wild shrews of the original breeding stock. In most local populations of the Asian shrews surveyed, Amy-1b was more common than Amy-1a. The Sri Lanka population was clearly distinguishable from the others, being nearly fixed with Amy-1a. The C band was found in eleven (one homozygous) of 86 wild shrews caught in Bangladesh. Of a total of 234 wild shrews collected from four Japanese and two Indonesian islands, Bangladesh, and Sri Lanka, only two showed different AMY-bands from AMY-A, -B and -C, and such bands were not found in the laboratory-bred shrews examined.     

Population Genetics of a Translocated Population of Mottled Ducks and Allies

Translocating species is an important management tool to establish or expand the range of species. Success of translocations requires an understanding of potential consequences, including whether a sufficient number of individuals were used to minimize founder effects and if interspecific hybridization poses a threat. We provide an updated and comprehensive genetic assessment of a 1970s–1980s translocation and now established mottled duck (Anas fulvigula) population in South Carolina, USA. In addition to examining the population genetics of these mottled ducks, we simulated expected genetic assignments for generational hybrids (F1–F10), permitting formal purity assignment across samples to identify true hybrids and establish hybridization rates. In addition to wild mallards (A. platyrhynchos), we tested for presence of hybrids with migrant American black ducks (A. rubripes) and released domestic game-farm mallards (A. p. domesticus). We used wild reference populations of North American mallard-like ducks and sampled game-farm mallards from 2 sites in South Carolina that could potentially interbreed with mottled ducks. Despite 2 different subspecies of mottled duck (Florida [A. f. fulvigula] and the Western Gulf Coast [A. f. maculatlus]) used in original translocations, we determined the gene pool of the Western Gulf Coast mottled duck was overwhelmingly represented in South Carolina's current population. We found no evidence of founder effects or inbreeding and concluded the original translocation of 1,285 mottled ducks was sufficient to maintain current genetic diversity. We identified 7 hybrids, including an F1 and 3 late-staged (i.e., F2–F3 backcrosses) mottled duck × black duck hybrids, 1 F2-mottled duck backcrossed with a wild mallard, and 2 F3-mottled ducks introgressed with game-farm mallard. We estimated a 15% hybridization rate in our mottled duck dataset; however, the general lack of F1 and intermediate hybrids were inconsistent with scenarios of high hybridization rates or presence of a hybrid swarm. Instead, our results suggested a scenario of infrequent interspecific hybridization between South Carolina's mottled ducks and congeners. We concluded that South Carolina's mottled duck population is sufficiently large now to absorb current hybridization rates because 85% of sampled mottled ducks were pure. These results demonstrate the importance in managing and maintaining large parental populations to counter hybridization. As such, future population management of mottled ducks in South Carolina will benefit from increased geographical and continued sampling to monitor hybridization rates with closely related congeners. We also suggest that any future translocations of mottled ducks to coastal South Carolina should originate from the Western Gulf Coast. © 2021 The Wildlife Society.     

Mottled ducks,feral mallards,and their hybrids in Florida

The nonmigratory and endemic Florida mottled duck (Anas fulvigula fulvigula) is facing conservation threats from the combined effects of urbanization and introgressive hybridization with feral mallards (Anas platyrhynchos) and mallard x mottled duck hybrids. In the past, the status of the Florida mottled duck population was assessed during annual aerial surveys and most brown ducks (mottled ducks, mallards, and hybrids of them) detected during the survey would have been mottled ducks. But the release of domesticated mallards for aesthetic purposes has led to increases in the prevalence of mallards-hybrids (mallards or mallard x mottled duck hybrids) throughout peninsular Florida, USA, and because it is impossible to differentiate among mottled ducks, female mallards, and hybrids during aerial surveys, helicopter surveys were halted in 2009 until state researchers could conduct a range-wide study to determine what proportion of brown ducks are mottled ducks versus mallards-hybrids. We used plumage keys and high-resolution photography to categorize brown ducks from 557 wetland grid points as either mottled ducks or mallards-hybrids. Of the 5,179 brown ducks categorized, 40.1% were mottled ducks and 59.9% were mallards-hybrids. We used logistic regression analysis to model the interactive effect of a site's latitude and level of urbanization (urban gradient value within a 2-km buffer) to generate a predictive raster surface (1-km resolution) of the study area with values corresponding to the probability that a brown duck observed within a cell is a pure mottled duck. Predicted values will be used as correction factors when estimating final mottled duck population abundance from brown-duck survey data. Additionally, the predictive raster surface will be used to identify wetlands where mottled ducks remain predominant so that these sites can be targeted for preservation. Overall, mallards-hybrids outnumbered mottled ducks throughout most of peninsular Florida, especially in more urbanized regions, and their current prevalence rate presents a serious conservation threat, via hybridization, to extant mottled duck populations.     

AMY-1 interacts with S-AKAP84 and AKAP95 in the cytoplasm and the nucleus,respectively, and inhibits cAMP-dependent protein kinase activity by preventing binding of its catalytic subunit to A-kinase-anchoring protein (AKAP) complex

We have reported that a novel c-Myc-binding protein, AMY-1, binds to cAMP-dependent protein kinase-anchoring protein 149 (AKAP149) and its splicing variant, AKAP84 and is localized in the mitochondria in a complex with RII, a regulatory subunit of cAMP-dependent protein kinase (PKA) (Furusawa, M., Ohnishi, T., Taira, T., Iguchi-Ariga, S. M. M., and Ariga, H. (2001) J. Biol. Chem. 276, 36647-36651). In this study, we further found that AMY-1 competitively bound to either AKAP95 or AKAP84 in the nucleus and the cytoplasm, respectively, in a concentration-dependent manner of either AKAP. Like AKAP84, AMY-1 was found to bind to the RII-binding region of AKAP95 in vivo and in vitro and to make a ternary complex with RII. It was also found that the formation of the complex of AMY-1 with AKAP84/95 and RII prevented a catalytic subunit from binding to this AKAP complex, leading to suppression of PKA activity. These findings suggest that AMY-1 is an important modulator of PKA.     

选育过程中的粤黄鸡血液淀粉酶（Amy—1）基因频率的世代变化

本文调查了粤黄鸡两个选育方向和交配方式均不同的品系的血液淀粉酶(Amy-1)各世代的分布情况,并以不同Amy-1类型的粤黄鸡作了交配试验。发现两个品系各世代都始终保持Amy-1分布不平衡状态,这种分布不平衡可能由各种Amy-1基因型生活力不同引起;另外,人工选择也可能造成Amy-1基因频率的改变。交配方式是否对Amy-1基因频率的改变起作用值得进一步研究。     

Genetics of hydroxyacid oxidase isozymes in the mouse: localisation of Hao-2 on linkage group XVI.

Electrophoretic variants of individual isozymes of L-alpha-hydroxyacid oxidase (HAOX-B4) and amylase (AMY-A) in an Asian subspecies of mouse, Mus musculus castaneus, have been used to localise the gene encoding the HAOX B subunit. The structural gene loci for these isozymes (Hao-2 and Amy-1) are apparently linked (4.9 +/- 2.4 per cent recombinants) in this organism, which places Hao-2 on linkage group XVI, since previous studies by Eicher and co-workers (1976) have localised Amy-1 on this chromosome.     

Assignment of LH XVI to chromosome 3 in the mouse

We have presented evidence that the mouse loci comprising linkage group XVI are located on chromosome 3 distal to the my locus such that the order of genes is: Car-1, Car-2--my--ma--soc--Amy-1, Amy-2--Va. The genetic length for chr 3 is now estimated to be 82 recombination units. The genetic location of the breakpoint in the reciprocal translocation T(2:3)24H is placed between the Amy-1 and Va loci. A new simplified method for determining the Amy-1 and Amy-2 genotype of mice is presented.     

Monomorphic anti-HLA-A,B,C monoclonal antibodies detecting molecular subunits and combinatorial determinants

Thirteen monoclonal antibodies that react with monomorphic determinants on the HLA-A,B,C-beta 2-microglobulin (beta 2m) molecule were characterized. Analysis of antibody activity included inhibition by papain-solubilized HLA antigens and free beta 2m, antibody binding to mouse-human somatic cell hybrids containing human chromosome 6 or 15, and antibody cross-reactivity with lymphocytes from nonhuman species. Two criteria for monomorphism were established: 1) equal inhibition or absorption of antibody activity by all papain-solubilized HLA antigens or cell lines of different HLA specificities tested; and 2) nonpolymorphic cross-reactivity within another species or subspecies. On the basis of soluble antigen inhibition and binding to somatic cell hybrids, 3 classes of antibodies were detected: anti-beta 2m, anti-heavy chain, and anti-complex (against a combinatorial determinant formed by heavy chain and beta 2m). Antibody cross-reaction patterns in nonhuman species were suggestive that these monomorphic antibodies detect a limited number of determinants, minimally one on each chain and 2 combinatorial determinants. Examination of the known primary sequences for HLA-A2, HLA-B7, H-2Kb, and mouse, rabbit and human beta 2m provides a molecular explanation for this limited mouse anti-HLA monomorphic antibody activity.     

Growth and survival trade-offs and outbreeding depression in rainbow trout (Oncorhynchus mykiss)

The purpose of this study was to examine, using a rainbow trout (Oncorhynchus mykiss) model system, the fitness consequences of three generations of introgression of genotypes adapted to two different environments (culture and nature). The experiments also isolated the influence of competitive interactions and risk of predation on the relative growth and survival of the wild and backcrossed lines. Line crosses representing fast-growing pure domestic (D), slow-growing pure wild (W), domestic x wild hybrids (F1), F1 x wild backcrosses (B1), and B1 x wild backcrosses (B2) were generated and reared under (1) culture conditions, (2) seminatural conditions with competition among genotypes, and (3) seminatural conditions under risk of predation. Survival of the fry in a seminatural environment with competition fit an additive model of gene action with the domestic fish having the highest survival and the wild fish the lowest, but under risk of predation outbreeding depression was suggested by low survival of the B2 lines. Evidence of a trade-off in growth and survival under risk of predation along with observations of genetically determined behavioral differences among the strains may provide some explanation for the observed differences in survival among the strains. This information is relevant to improving our evolutionary understanding of the interaction among genomes, and the influence of environment, during hybridization events. Results from this experiment indicate that alteration of phenotype likely played a prominent role in the reduced fitness experienced by progeny produced after three generations of introgression, supporting the theory that disruption of genotypes selected for adaptation to local conditions may be a primary cause of outbreeding depression in species such as salmon.     

Comparative histopathological characteristics of highly pathogenic avian influenza (HPAI) in chickens and domestic ducks in 2008 Korea

We compared characteristic lesions occurring in chickens and domestic ducks naturally infected with H5N1 HPAI virus in April and May 2008. Infected chickens generally exhibited pale-green, watery diarrhoea, depression, neurological signs and cyanosis of wattles and combs, and infected ducks generally exhibited neurological signs and watery diarrhoea. Gross petechial or ecchymotic haemorrhage affected the heart, proventriculus, liver, muscle, fat, and pancreas in chickens, and muscle in ducks. Necrotic foci were primarily present in the pancreas of both species and in the heart of domestic ducks. Histopathologically, chickens exhibited multifocal encephalomalacia, multifocal lymphohistiocytic myocarditis, multifocal necrotic pancreatitis and haemorrhage of several organs and tissues; ducks exhibited lymphohistiocytic meningoencephalitis with multifocal haemorrhages, multifocal necrotic pancreatitis, and severe necrotic myocarditis with mineralisation. The characteristic histopathologic findings of 2008 HPAI were multifocal encephalomalacia and necrotic pancreatitis accompanied by lymphohistiocytic myocarditis, and haemorrhage in various organs and tissues in chickens, whereas in ducks, they were severe necrotic myocarditis with mineralisation and necrotic pancreatitis, accompanied with lymphohistiocytic meningoencephalitis. The high mortality of domestic ducks may be intimately associated with heart failure resulting from increased H5N1 HPAI viral cardiotropism.     

林麝和马麝随机扩增多态DNA的研究

用随机扩增多态 DNA(RAPD)技术对饲养的林麝和马麝进行分子遗传标记研究。在选用的42 种随机引物中, 有25种引物产生了清晰稳定的条带, 单个引物获得标记数在1～14 之间,平均每个个体获得168个RAPD标记 , 其中林麝、马麝特异性标记各5个,个体特异性标记有3个, 这些标记可用来鉴定种或个体。平均遗传距离在林麝种内为0.27±0.023, 马麝为0.105±0.013, 种间为0.241±0.02 , 种间差异显著大于种内差异。分析表明饲养马麝种内遗传多样性低, 为增强饲养马麝的生存力, 最好从不同种群中引入种麝进行繁殖。     

Simultaneous expression of salivary and pancreatic amylase genes in cultured mouse hepatoma cells.

The tissue-specific expression of two types of mouse amylase genes does not overlap in vivo; the Amy-1 locus is transcribed in the parotid gland and the liver, while expression of Amy-2 is limited to the pancreas. We identified a mouse hepatoma cell line, Hepa 1-6, in which both amylase genes can be simultaneously expressed. Amy-1 is constitutively active in these cells and is inducible by dexamethasone at the level of mRNA. We demonstrated that the liver-specific promoter of Amy-1 is utilized by the dexamethasone-treated hepatoma cells, and that glucocorticoid consensus sequences are present upstream of this promoter. Amy-2 is not detectable constitutively, but can be activated if the cells are cultured in serum-free medium containing dexamethasone. Expression of Amy-2 in a nonpancreatic cell type has not previously been observed. We speculate that induction of Amy-1 and activation of Amy-2 may involve different regulatory mechanisms. Hepa 1-6 cells provide an experimental system for molecular analysis of these events.