ABSTRACT: Determination of Genomic Markers to Conduct Parentage, Differentiate Wood and Plains Bison Sub-species, and Measure Cattle Introgression in Canadian Bison
Project description:The project aimed to determine genomic markers to conduct parentage, differentiate wood and plains bison sub-species, and measure cattle introgression in American bison
Project description:These arrays measure gene expression across eight Y introgression lines in Drosophila simulans. Four lines (Ya19, Ya23, Ya24, Ya26) carry a D. simulans Y chromosome (from a Cameroon population) and four lines (Sec01, Sec03, Sec08, Sec27) carry a D. sechellia Y chromosome. All lines are otherwise identical with a D. simulans background (UCSD stock center line 14021-0251.092).
Project description:The vascular cambium is responsible for the production of secondary xylem, which comprises the most abundant form of biomass on earth, wood. Despite its massive global importance, the regulatory networks underlying the production of secondary xylem remain partially ambiguous. Countless studies have used whole-tissue (bulk) RNA sequencing (RNA-seq) to characterize transcriptome changes during wood development in Populus and other tree genera. These studies were limited by their resolution and regulatory inferences. In contrast, novel single-cell RNA sequencing (scRNA-seq) technologies provide opportunities to gain insight into the transcriptional program that controls cellular lineages as they differentiate to form the various cell types in wood. In this study, scRNA-seq was carried out utilizing a pool of 11,673 nuclei derived from two replicates of stem samples of Populus trichocarpa to create a single-cell transcriptome atlas with an unprecedented resolution for a tree species. Cell-type specific marker genes were utilized to annotate 20 cell clusters representing the known cell types within the sampled tissue. Reporter gene assays were performed to confirm the cluster-specific cell-type identity of vessel elements, fibers, ray parenchyma, cambial cells, and sub-cell type vessel-associated cells. The developmental trajectory of cambial cells and their xylem-specific derivates was implemented to identify putative regulators that control distinct developmental lineages involved in vascular development and xylogenesis. Finally, an integration with a protoplast derived, single-cell, whole stem dataset was conducted to compare the proficiency of each methodology to capture the transcriptome.