Billy Muro, Dr. Clint Löest Lab, Animal & Range Sciences
“My Project focuses on the effects of glycerol in rumen bacteria. We are measuring VFA content produced by rumen bacteria with various levels of glycerol concentration. We are also going to see the potential to develop a supplement to negate the negative feedback glycerol has on ammonium and nitrogen retention”.
Clara Maxam, Dr. Ryan Ashley Lab, Animal & Range Sciences
“Immunological changes after inhibiting chemokine receptor 4 (CXCR4) at the fetal-maternal interface in sheep were investigated. Osmotic pumps containing CXCR4 inhibitor or saline (control) were surgically installed to deliver treatments into the ovine uterus. Blood was collected daily and spleen tissue collected at necropsy on days 20 and 35 of gestation for mRNA analysis. Compared to control, TGFB1 expression rose on day 14 and IL10 declined on day 26 in peripheral blood. In spleen from treated ewes, TGFB1 increased while IL10 decreased on days 20 and 35, respectively. These results indicate disrupting CXCR4 signaling in the uterus affects peripheral immunity”.
Carlos Campos, Dr. Tim Wright Lab, Biology
“My research focuses on Blue-Throated Macaw conservation genetics. We use Polymerase-Chain Reaction to amplify genetic markers such as polymorphic microsatellite loci and mitochondrial DNA. We plan on testing for population structure, divergence, and pedigree as well as the presence of a population bottleneck and the presence of inbreeding and inbreeding depression”.
David Rodriguez, Dr. Kevin Houston Lab, Chemistry & Biochemistry
“Fluorescence lifetime is being related to different cell metabolic pathways such as glycolysis. Fluorescence lifetime value differs when cancer cells are sensitive to a specific drug. On my research, tamoxifen is used to measure sensitivity at different doses for breast cancer cells. Also, we are looking for which metabolism it is faster or if it does depends on the treatment and the cell line and how it is related to fluorescence lifetime values”.
Trung Nguyen, Dr. Barbara Lyons Lab, Chemistry & Biochemistry
“Fibrolamellar Hepatocellular Carcinoma (FL-HCC) is a rare and aggressive liver cancer subtype that almost exclusively occurs in adolescents. It is believed to be caused by a mutation that results in a fusion (chimera) protein between the heat shock protein DNAJB1, and protein kinase A (PKA or PRKACA). Nevertheless, little progress has been made in characterizing the fusion protein DNAJB1-PRKACA’s role due to the rarity of FL-HCC. I am currently working towards characterizing the fusion protein in terms of its structural features to understand how differently it interacts with its targets in cancer cells in comparison to those of normal PKA in healthy cells. Last but not least, of particular interest is also the pathological role that the chimera protein has from a cell molecular biology and genetics viewpoint”.
Frederick Hansen, Dr. Nicole Pietrasiak Lab, Plant & Environmental Sciences
“The distribution patterns of soil microbes living independent of vascular plants are poorly understood, especially so in desert ecosystems. Soil microbes and biological soil crusts which are living aggregates containing bacteria, cyanobacteria, algae, fungi and other components, provide important ecosystem services to desert habitats. In my research I am investigating the microbial diversity of soil surfaces in the intershrub area of the five main vegetative zones within the Jornada Basin located in Southern New Mexico, using genetic and physical techniques. To understand the diversity and drivers of microbial diversity within the soils, I studied the abiotic and biotic characteristics of the soils within the various sites and hope to test various soil characteristics such as pH, electrical conductivity, moisture, and texture for their effect on microbial diversity. Understanding the ecosystem’s soil microbial diversity and diversity drivers will help in preserving and restoring areas that are vulnerable to disturbance or change”.
Prisila Ramirez, Dr. Amanda Ashley Lab, Chemistry & Biochemistry
Assessing the Role of Senataxin Mutations and R-Loops in ALS4. Senataxin (SETX) is a RNA-DNA helicase that resolves R-loops by unwinding the RNA-DNA hybrid, allowing DNA to regain its double-stranded conformation. Heterozygous mutations in SETX are responsible for the juvenile form of amyotrophic lateral sclerosis (ALS4). Recently, our lab demonstrated that individuals with the L389S SETX missense mutation have lower R-loop levels when compared to non ALS4 individuals.