bioRxiv Science⌕ Search

Biology subjects

Conley, E.

Publications and source records attributed to Conley, E..

2 recordsLinked to original sources

A century of breeding has preserved genetic variation, accumulated favorable alleles, and shaped the Rht gene portfolio in North American spring wheat

Hard red spring wheat (HRSW) is an important market class of wheat in North America with a rich history of breeding. We genotyped 1,013 HRSW lines representing a century of breeding material using a SNP array and targeted KASP genotyping to assess the changes in genetic diversity and Rht genes in HRSW from North America. Results show that early breeding efforts broadened an initially narrow gene pool derived from a few founders and subsequently maintained the genetic diversity. Analysis of Rht genes revealed that Rht-D1b was the predominant semi-dwarf allele from introduction of the Green Revolution genes (Rht-B1 and Rht-D1) in 1960s until the FHB epidemics of 1990s, when most breeding programs shifted to Rht-B1b. However, adoption of Rht-B1b and Rht-D1b remains low in some regions of the Great Plains. The dwarf alleles at GA-sensitive Rht24 and Rht25 have persisted in the region at low frequencies before the introduction of Green Revolution genes and have increased in frequency in recent decades. We also analyzed the effect of Rht genes on plant height (PH) in the HRSW growing region and found that Rht-B1b or Rht-D1b results in [~]12% reduction in PH, which decreases to [~]9% in dry environments. Notably, combining dwarfing alleles at Rht24 and Rht25 reduced height by [~]6% in dry environments, suggesting an alternative approach for reducing PH. Our analysis also revealed significant genetic interactions between Rht-B1 and Rht25, as well as between Rht-D1 and Rht24, which could help fine-tune PH for different environments by employing appropriate Rht combinations. Furthermore, our results demonstrate positive selection for photoperiod sensitivity in recent decades, particularly in high-latitude regions. This study provides a valuable genomic resource, and the findings enhance our understanding of past breeding efforts while offering insights to guide future plant breeding strategies.

plant biology↗

The C. albicans virulence factor Candidalysin polymerizes in solution to form membrane pores and damage epithelial cells.

The pathogenic fungus Candida albicans causes severe invasive candidiasis. C. albicans infection requires the action of the virulence factor Candidalysin (CL), which damages the plasma membrane of the target human cells. However, the molecular mechanism that CL uses to permeabilize membranes is poorly understood. We employed complementary biophysical, modeling, microscopy, and cell biology methods to reveal that CL forms membrane pores using a unique molecular mechanism. Unexpectedly, it was observed that CL readily assembles into linear polymers in solution. The basic structural unit in polymer formation is a CL 8-mer, which is sequentially added into a string configuration. Finally, the linear polymers can close into a loop. Our data indicate that CL loops spontaneously insert into the membrane to become membrane pores. We identified a CL mutation (G4W) that inhibited the formation of polymers in solution and prevented formation of pores in different synthetic lipid membranes systems. Studies in epithelial cells showed that G4W CL failed to activate the danger response signaling pathway, a hallmark of the pathogenic effect of CL. These results indicate that CL polymerization in solution is a necessary step for the damage of cellular membranes. Analysis of thousands of CL pores by atomic force microscopy revealed the co-existence of simple depressions and complex pores decorated with protrusions. Imaging and modeling indicate that the two types of pores are formed by CL molecules assembled into alternate orientations. We propose that this structural rearrangement represents a maturation mechanism that might stabilize pore formation to achieve more robust cellular damage. Taken together, the data show that CL uses a previously unknown mechanism to damage membranes, whereby pre-assembly of CL loops in solution directly leads to formation of membrane pores. Our investigation not only unravels a new paradigm for the formation of membrane pores, but additionally identifies CL polymerization as a novel therapeutic target to treat candidiasis.

biophysics↗