Expression and inheritance of perenniality and other qualitative traits in hybrids between mungbean cultivars and Australian wild accessions

2012 ◽  
Vol 63 (7) ◽  
pp. 619 ◽  
Author(s):  
Thuan D. Nguyen ◽  
R. J. Lawn ◽  
L. M. Bielig

The expression and inheritance of several qualitative traits was examined in four cultivated × wild hybrid populations involving each of two mungbean (Vigna radiata ssp. radiata) cultivars, cvv. Berken and Kiloga, and each of two Australian accessions of the wild subspecies (V. radiata ssp. sublobata). One of the wild accessions, ACC 1, was representative of a prostrate, fine-stemmed, gracile type and the other, ACC 87, was representative of a more robust perennial form endemic in north-eastern Australia. For each of the four cultivated × wild populations, trait expression was observed in plants from the parent, F1, F2, and the two F1–parental backcross generations, when grown under favourable conditions in large pots on benches in the field at CSIRO Davies Laboratory, Townsville, Australia. Models of inheritance were inferred based on the segregation patterns in the different generations of the cultivated v. wild phenotypes. For most traits, the model of inheritance depended more on the wild than the cultivated parent, with more traits in the crosses involving ACC 1 being digenic than in those involving ACC 87. For all the observed morphological and seed traits, the wild phenotype was dominant, consistent with the cultivated phenotype having arisen through mutations that inhibited expression of the wild type. In contrast, the apparent resistance of the wild parents to field strains of powdery mildew disease was recessive to the strong susceptibility of the two cultivars. The segregation patterns for presence or absence of tuberous roots were remarkably similar in the two crosses involving the perennial accession ACC 87, and were consistent with the formation of tuberous roots being conditioned by two complementary, dominant genes. The fact that an apparently complex trait like perenniality might be conditioned by so few genes suggested that perenniality may also be an ancestral wild trait, disruption of which has led to the now more common, annual form. Linkage analyses suggested that perenniality was associated with the wild-type seed traits, black speckled testa and pigmented hilum, which previous molecular studies have indicated are both located on mungbean linkage group 2.

Phytotaxa ◽  
2013 ◽  
Vol 133 (1) ◽  
pp. 1 ◽  
Author(s):  
GLENN B. MCGREGOR

This volume provides the first detailed account of the Chroococcales of north-eastern Australia. It provides keys, morphological and ecological data for 6 families, 33 genera and 112 species, and photomicrographs and original illustrations to enable the identification of natural populations based on stable and recognizable characters observable with the aid of light microscopy. Distributional data are based on extensive surveys at 270 sites representing the major freshwater habitats including rivers and streams, palustrine and lacustrine wetlands, thermal springs, and man-made reservoirs in Queensland and the Northern Territory as well as a review of the Australian phycological literature. 


2016 ◽  
Vol 36 (suppl_1) ◽  
Author(s):  
Jochen Steppan ◽  
Ivy Wang ◽  
Yehudit Bergman ◽  
Siqi Tan ◽  
Sandeep Jandu ◽  
...  

Introduction: Stiffening of the central vasculature is a strong and independent predictor of adverse cardiovascular events. Vascular stiffening is a complex process that involves changes in the vessel wall composition and smooth muscle cell (SMC) function. We recently used an unbiased proteomic approach to identify Lysyl oxidase like 2 (LOXL2) as a potential new target in vascular stiffness. The goal of this study is to characterize the role of LOXL2 in vascular stiffening and its potential as a target to reverse vascular stiffness associated with hypertension. Results: We demonstrate that decreased nitric oxide (NO) bioavailability results in increased secretion and activity of LOXL2 in SMCs. LOXL2 knockdown markedly attenuates SMC adhesion, motility, and proliferation and results in diminished matrix deposition. LOXL2 knockdown also results in striking changes in the stiffness and cytoskeletal remodeling events in CMSs. Tensile testing shows that intact aortas of LOXL2+/- animals are stiffer when compared with those from wild type mice, while there is no difference in decellularized vessels. We next investigated the role of LOXL2 in the development of hypertension using angiotensin II (AngII) infusion in LOXL2+/- (group 1) and wild type (WT; group 2) mice. BP and pulse wave velocity (PWV) increased significantly with AngII infusion in both groups during the study period, without a significant change in heart rate. Compared to WT animals, contractile responsiveness was markedly diminished in LOXL2+/- animals at baseline as well as with AngII infusion when compared with untreated controls. The NO- dependent vasodilatory response to acetylcholine was identical at baseline and diminished significantly with AngII infusion in both groups of animals. There was no difference between the groups in the endothelium-independent response to sodium nitroprusside. Conclusion: In this study, we demonstrated the role of NO in the regulation of LOXL2. Interestingly, LOXL2 appears to have a dual role in vascular stiffness by affecting both SMC function as well as matrix composition. We therefore conclude that LOXL2 is a novel target involved in vascular stiffness that requires further characterization to elicit the possibility of therapeutic intervention.


2021 ◽  
Vol 23 (Supplement_6) ◽  
pp. vi97-vi97
Author(s):  
Stefaan Van Gool ◽  
Jennifer Makalowski ◽  
Volker Schirrmacher ◽  
Wilfried Stuecker

Abstract The prognosis of IDH1 wild type MGMT promotor unmethylated (MGMT-p-UM) GBM patients remains poor. Addition of TMZ to radiotherapy shifted the median OS from 11.8 to 12.6 months (Stupp, Lancet Oncol 2019). We retrospectively analysed the value of individualized multimodal immunotherapy (IMI) to improve OS in these patients. Adults with first event of IDH1wt GBM and documented status of MGMT-p-UM, and treated with IMI in the period June 2015 till July 2020, were selected. IMI consisted of 1/ immunogenic cell death (ICD) therapy (NDV injections + modulated electrohyperthermia), 2/ active specific immunotherapy with autologous mature dendritic cells loaded with tumor lysate or ICD therapy-induced serum-derived antigenic extracellular microvesicles and apoptotic bodies (IO-Vac® is an approved advanced therapy medicinal product since 27/05/2015), 3/ modulatory immunotherapy adapted to the patient, and 4/ complementary medicines. Twenty-eight patients (11f, 17m) had a median age of 48y (range 18-69) and a KPI of 90 (50-100). Extent of resection was complete (11), < complete (9) or not documented (8). Seven patients were treated with surgery/radio(chemo)therapy and subsequent IMI (Group-1); 21 patients were treated with radiochemotherapy followed by maintenance TMZ + ICD therapy, followed by DC vaccines (Group-2). Both groups received further maintenance ICD therapy. Age, KPI and extent of resection were not different amongst both groups. PFS was not assessed because of challenges about pseudoprogression. The median OS of group-1 patients was 11m (2y OS: 0%). Surprisingly the median OS of group-2 patients was 18m with 2y OS of 17% (CI95%: +31, -15), which was significantly (Log-rank: p = 0.027) different from group-1. The data suggest that addition of IMI after local therapy on its own has no relevant effect on OS in IDH1 wild type MGMT-p-UM GBM patients, similar to maintenance TMZ. However, the combination of both TMZ + IMI significantly improves median OS.


1999 ◽  
Vol 50 (2) ◽  
pp. 159 ◽  
Author(s):  
D. Walker

Lakes Barrine and Eacham, ~1.0 and 0.5 km2 area, 67 and 63 m depth respectively, lie at ~740 m a.s.l., ~17°S in north-eastern Australia. Seasonal changes in their volumes modelled from meteorological data correspond well with observations at Eacham. Temperature profiles through 6 years show summer stratification with a metalimnion at 20–30 m; in winter, near isothermy is usually attained. At Barrine, thermal stability varies between winter and summer (<500 and >4000 g-cm cm-2 respectively). Mixing is related to low ground temperatures during periods of generally low thermal stability; exceptionally it penetrates to >60 m. Oxygen saturation decreases from the surface to ~20% at the base of the euphotic zone (15–21 m) but oxygen is carried lower by mixing after which anoxia commonly rises to ~40 m. At Barrine, Fe-reducing redox (<200 mV) usually occurs below 50 m, but during mixing this boundary falls to within 1 m of the mud–water interface. The Barrine solution is dilute (total dissolved solids 55–58 mg L-1), and that of Eacham is more so. A concentrated monimolimnion has developed in the lowermost 2–3 m at Barrine but not at Eacham. Sedimentation at the middle of each lake results from the continuous deposition of open-water products punctuated by the redistribution of coarser detritus from the ‘shallows’ at times of deep mixing. The resultant laminations are preserved only at Barrine, protected by the chemical stability of the monimolimnion.


2019 ◽  
Author(s):  
Teresa W. Lee ◽  
Heidi S. David ◽  
Amanda K. Engstrom ◽  
Brandon S. Carpenter ◽  
David J. Katz

ABSTRACTDuring active transcription, the COMPASS complex methylates histone H3 at lysine 4 (H3K4me). In Caenorhabditis elegans, mutations in COMPASS subunits, including WDR-5, extend lifespan and enable the inheritance of increased lifespan in wild-type descendants. Here we show that the increased lifespan of wdr-5 mutants is itself a transgenerational trait that manifests after eighteen generations and correlates with changes in the heterochromatin factor H3K9me2. Additionally, we find that wdr-5 mutant longevity and its inheritance requires the H3K9me2 methyltransferase MET-2 and can be recapitulated by a mutation in the putative H3K9me2 demethylase JHDM-1. These data suggest that lifespan is constrained by reduced H3K9me2 due to transcription-coupled H3K4me. wdr-5 mutants alleviate this burden, extending lifespan and enabling the inheritance of increased lifespan. Thus, H3K9me2 functions in the epigenetic establishment and inheritance of a complex trait. Based on this model, we propose that lifespan is limited by the germline in part because germline transcription reduces heterochromatin.


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