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Biology subjects

Veregge, M. L.

Publications and source records attributed to Veregge, M. L..

2 recordsLinked to original sources

Rye stem rust is a reservoir of diversity and virulence for wheat stem rust

Sexual populations of the stem rust pathogen (Puccinia graminis or Pg) are producing new race types globally. An analysis of 385 Pg genomes (204 from this study) illuminated international migration and admixture events. Within Kazakhstan, a novel and diverse sexual clade of P. graminis is described. An analysis of the highly divergent mating type homeodomain (HD) locus found that the 75 Kazakhstan isolates had 41 different HD haplotypes, out of a total of 99 P. graminis HD haplotypes found globally. Kazakh isolates share HD haplotypes with isolates in clade 1 (Ug99), 3-B (TTRTF), and 4 (TKTTF). There are 148 unique combinations of HD locus haplotypes within the 385 isolates. Rye (Pgs) and wheat (Pgt) stem rust share multiple HD locus haplotypes and have conserved pheromone receptors and precursors, while oat stem rust (Pga) does not. Virulent alleles for AvrSr13, AvrSr22, and AvrSr50 in Pgt are frequently derived from admixture with Pgs. Pgs also contains virulent effectors for AvrSr33, AvrSr62, and AvrSr27. Pgt isolates virulent on Sr31, such as Ug99 and isolates from Spain, have genetic links to North American Pgs isolates which are present in regions of the United States where barberry is common.

plant biology↗

A single cell atlas of human and mouse white adipose tissue

White adipose tissue (WAT), once regarded as morphologically and functionally bland, is now recognized to be dynamic, plastic, heterogenous, and involved in a wide array of biological processes including energy homeostasis, glucose and lipid handling, blood pressure control, and host defense1. High fat feeding and other metabolic stressors cause dramatic changes in adipose morphology, physiology, and cellular composition1, and alterations in adiposity are associated with insulin resistance, dyslipidemia, and type 2 diabetes (T2D)2. Here, we provide detailed cellular atlases of human and murine subcutaneous and visceral white fat at single cell resolution across a range of body weight. We identify subpopulations of adipocytes, adipose stem and progenitor cells (ASPCs), vascular, and immune cells and demonstrate commonalities and differences across species and dietary conditions. We link specific cell types to increased risk of metabolic disease, and we provide an initial blueprint for a comprehensive set of interactions between individual cell types in the adipose niche in leanness and obesity. These data comprise an extensive resource for the exploration of genes, traits, and cell types in the function of WAT across species, depots, and nutritional conditions.

physiology↗