Robert Wayne, Ph.D.

I consider myself a generally trained evolutionary biologist with a wide interest in a range of problems spanning the fields of evolutionary biology, ecology, behavior, and biological conservation. Current projects in my lab include genomics of opossums, dolphins, zebra, bobcats, bats, birds and abalone, but I am perhaps best known for evolutionary and population genetic studies on domestic dogs and wolves. I am fond of cutting-edge technology and methods of analysis, and my lab currently focuses on complete genome sequencing and gene expression analysis using next generation sequencing platforms. Some of our primary interests include identifying genes involved in local adaptation and their relationship to phenotype and behavior. Along with Tim Coulson at Oxford, we are attempting to model the genotype-gene expression-phenotype map in wolves and its influence on population dynamics. Complementing this modeling approach, we are generating empirical data on allele-specific expression in genes under selection in natural populations using cell culture in which controlled manipulations can be done. We have also focused on large scale resequencing studies of candidate genes in natural populations using sequence capture arrays, analyzing as much as 16 million bp per individual in a sample of over 400 wolves. We are also currently analyzing over 100 genomes from domestic and wild canids to reconstruct demographic history and patterns of variation along the genome, including adaptive and deleterious variation.

A long-standing interest of mine is using new approaches to address problems in biological conservation, and specifically, how gene expression enables a rapid, first line response to climate change. For example, my students are assessing gene expression responses to stressors in wolves as a function of habitat disturbance and as a function of toxicants and petroleum derivatives in dolphins in near-shore environments. I encourage new students to develop their own projects that follow their specific interests and passions and address fundamental questions. This often results in students working in areas somewhat distant from my fields of expertise, but I am open to nearly any topic in evolutionary biology as long as there is a common thread of molecular genetic techniques. UCLA provides very competitive fellowships, but I expect students to endeavor to raise support especially for field or lab work outside of the scope of current supported projects. Being bold in constructing a novel PhD project that goes beyond existing projects in my lab is a critical exercise that is fundamental to students becoming independent, creative researchers.

Rachelle Crosbie-Watson, Ph.D.

Research Interests
My research program focuses on determining the pathogenetic mechanisms of muscular dystrophy. Members of the lab are examining the muscle function using biochemical, molecular, and cellular approaches. There are many forms of muscular dystrophy caused by primary genetic mutations within different muscle genes. For instance, mutations in dystrophin are responsible for causing Duchenne muscular dystrophy (DMD) while mutations in any of the four sarcoglycan genes cause limb-girdle muscular dystrophy. Congenital and Emery-Dreyfus muscular dystrophies are caused by mutations in laminin and emerin, respectively. These muscle diseases differ based on the types of muscles that are affected, clinical progress of the disease, and mode of inheritance. My lab is interested in 1) determining why these proteins are critical for normal muscle function 2) creating animal models for specific forms of muscular dystrophy using transgenic and knockout mouse technology and 3) developing new therapeutic agents. We are in the process of testing FDA-approved compounds in mouse models of muscular dystrophy. In addition, we are developing novel animal models for muscle proteins that are known to rescue muscular dystrophy.
Biography

Dr. Crosbie-Watson has pioneered work on the function of sarcospan within the dystrophin-glycoprotein complex. Introduction of sarcospan into dystrophin-deficient mice ameliorates muscular dystrophy in a me. The Crosbie lab has generated all the molecular tools and reagents for the study of sarcospan, which are not available elsewhere. Building on expertise in sarcospan and the dystrophin-glycoprotein complex, the Crosbie lab is collaborating with the Baum lab in development of HTS assays to detect alteration in sarcospan expression as a therapy for Duchenne Muscular Dystrophy. Dr. Crosbie has also collaborated with the Spencer group at UCLA to develop and characterize novel methodologies for creating mouse models of muscle disease. In addition to her research, Dr. Crosbie is a dedicated educator. She has trained several HHMI, Beckman, and Dean’s undergraduate and graduate scholars. She successfully mentored a successful recipient of the prestigious Marshall Scholarship. This student was one of only thirteen students to be awarded the Marshall in UCLA?s history. Based on her excellence in classroom instruction, Dr. Crosbie was nominated for a Teaching Distinction Award at UCLA and she is Faculty Director of the Beckman Undergraduate Scholars Program.

Aradhna Tripati, Ph.D.

Aradhna Tripati grew up in Los Angeles and when she was in college, took a general education course on Environmental Geology that ignited her passion for environmental science and geoscience. She researches and teaches about climate change; the history and dynamics of changing Earth systems including climate, ice sheets, oceans, the water cycle, carbon dioxide levels; tool development; and clumped isotope geochemistry. She is now Associate Professor in the Institute of the Environment and Sustainability (IoES), the Department of Atmospheric and Oceanic Sciences, the Department of Earth, Planetary, and Space Sciences, the Institute for Geophysics and Planetary Physics (IGPP), and the California Nanosystems Institute (CNSI), as her work is highly interdisciplinary.

Aradhna also is the faculty director and founder of the Center for Diverse Leadership in Science. She has mentored, advised, co-advised, trained, or served on the committee for over 130 postdoctoral fellows and researchers, Ph.D. students, M.S. students, undergraduates, high school teachers, and high school students. Aradhna has over 3000 citations for her research, and has established world-renowned laboratories. She has 66 publications of which 12 are in Nature journals, Science, or Proceedings of the National Academy of Sciences, 181 conference abstracts, 13 invited talks and three keynote lectures at international conferences, and 50 invited talks at universities and research institutes. Her lifelong goals include advancing new geochemical tracers for the study of Earth system processes, studying the history and dynamics of climate change, and working to educate, recruit, and retain a diverse population into environmental science and geoscience, and more generally in higher education.

Aradhna has received numerous awards for her research, education, and outreach programs including a Presidential Early Career Award in Science and Engineering from President Obama and the White House Office for Science, Technology, and Policy, and the National Science Foundation’s CAREER award, NSF’s most prestigious award in support of early career faculty who exemplify the role of teacher-scholars through outstanding research, excellent education and the integration of education and research within the context of the mission of their organizations. She received the Bromery Award for Minorities from the Geological Society of America. Aradhna has been named a Hellman Fellow and a National Academy of Sciences Kavli Fellow, and recently received the E.O. Wilson Award for Outstanding Science on climate change. She also was awarded a Chair International D’Excellence in Stable Isotopes by IUEM (Institut Universitaire European De La Mer).

She received her B.S. in Geological Sciences from California State University, Los Angeles where she received the Aaron Waters Award for Outstanding Senior. Aradhna received her Ph.D. in Earth Sciences at UC Santa Cruz where she was a Gates Millennium Scholar, an Ocean Drilling Program Fellow, and a UC Regents’ Fellow – and she received the Aaron Waters Award for Best Thesis Proposal. She was a research fellow at the University of Cambridge where she held the Thomas Nevile Fellowship in Natural Sciences, a Comer Abrupt Climate Change Fellowship, a National Environmental Research Council Fellowship, and a Marshall Sherfield Fellowship. Aradhna also was a visiting scientist at the California Institute of Technology for several years. She began as an assistant professor at UCLA in 2009 and received tenure in 2014.

Alvaro Sagasti, Ph.D.

Research Interests
Morphogenesis is the process by which cells adopt their specific shapes, sizes, and relationships with neighboring cells. Our lab studies the morphogenesis of developing skin cells and sensory neurons, which together mediate touch sensation. The skin at early developmental stages consists of two epithelial layers, each with distinct functions and morphologies. Sensory neurons project elaborately branched cellular processes called peripheral axons into the territory between the two skin layers to detect touch stimuli. We investigate how each of these cell types adopts its distinct morphological features and how skin cells and neurons influence each other’s morphogenesis. To study these questions we use zebrafish embryos and larvae as a model. Because zebrafish eggs are externally fertilized and their embryos are optically clear, cellular behaviors can be imaged in live animals. Transgenic lines allow us to visualize specific cells and subcellular processes, laser-based techniques allow us to damage cells at precise times and places to study repair, and genetic manipulations provide insight into the molecular underpinnings of cellular behaviors. By studying basic cellular processes we hope to shed light on how they are impacted by damage and disease.
Biography

 

Dr. Sagasti received his PhD from UCSF, where he worked with Cori Bargmann studying celll specification and left/right asymmetry in the nervous system of the nematode C. elegans. He began using zebrafish as a model at the Skirball Institute, NYU Medical Center as a post-doc with Alex Schier. In the summer of 2005 he was a Grass Foundation Fellow at the Marine Biological Labs in Woods Hole, Massachussetts. He began as a UCLA faculty member in the MCDB department in September 2005. His lab uses a combination of imaging, molecular, and genetic approaches in zebrafish to investigate on the morphogenesis of sensory axons and skin cells during development and repair.

 

Publications

A selected list of publications:

Vargas Mauricio Enrique, Yamagishi Yuya, Tessier-Lavigne Marc, Sagasti Alvaro   Live Imaging of Calcium Dynamics during Axon Degeneration Reveals Two Functionally Distinct Phases of Calcium Influx The Journal of neuroscience : the official journal of the Society for Neuroscience, 2015; 35(45): 15026-38.
Rasmussen Jeffrey P, Sack Georgeann S, Martin Seanna M, Sagasti Alvaro   Vertebrate epidermal cells are broad-specificity phagocytes that clear sensory axon debris The Journal of neuroscience : the official journal of the Society for Neuroscience, 2015; 35(2): 559-70.
O’Donnell Kelley C, Lulla Aaron, Stahl Mark C, Wheat Nickolas D, Bronstein Jeff M, Sagasti Alvaro   Axon degeneration and PGC-1α-mediated protection in a zebrafish model of α-synuclein toxicity Disease models & mechanisms, 2014; 7(5): 571-82.
O’Donnell Kelley C, Vargas Mauricio E, Sagasti Alvaro   WldS and PGC-1α regulate mitochondrial transport and oxidation state after axonal injury The Journal of neuroscience : the official journal of the Society for Neuroscience, 2013; 33(37): 14778-90.
Palanca Ana Marie S, Lee Sung-Ling, Yee Laura E, Joe-Wong Carlee, Trinh Le A, Hiroyasu Elizabeth, Husain Majid, Fraser Scott E, Pellegrini Matteo, Sagasti Alvaro   New transgenic reporters identify somatosensory neuron subtypes in larval zebrafish Developmental neurobiology, 2013; 73(2): 152-67.
Wang Fang, Wolfson Sean N, Gharib Arash, Sagasti Alvaro   LAR receptor tyrosine phosphatases and HSPGs guide peripheral sensory axons to the skin Current biology : CB, 2012; 22(5): 373-82.
Villegas Rosario, Martin Seanna M, O’Donnell Kelley C, Carrillo Simon A, Sagasti Alvaro, Allende Miguel L   Dynamics of degeneration and regeneration in developing zebrafish peripheral axons reveals a requirement for extrinsic cell types Neural development, 2012; 7(6): 19.
Martin Seanna M, O’Brien Georgeann S, Portera-Cailliau Carlos, Sagasti Alvaro   Wallerian degeneration of zebrafish trigeminal axons in the skin is required for regeneration and developmental pruning Development (Cambridge, England), 2010; 137(23): 3985-94.
O’Brien Georgeann S, Martin Seanna M, Söllner Christian, Wright Gavin J, Becker Catherina G, Portera-Cailliau Carlos, Sagasti Alvaro   Developmentally regulated impediments to skin reinnervation by injured peripheral sensory axon terminals Current biology : CB, 2009; 19(24): 2086-90.
Sagasti, A Guido, MR Raible, DW Schier, AF.   Repulsive interactions shape the morphologies and functional arrangement of zebrafish peripheral sensory arbors Current biology , 2005; 15(9): 804-14.
O’Brien Georgeann S, Rieger Sandra, Wang Fang, Smolen Gromoslaw A, Gonzalez Robert E, Buchanan JoAnn, Sagasti Alvaro   Coordinate development of skin cells and cutaneous sensory axons in zebrafish The Journal of comparative neurology, 2012; 520(4): 816-31.
Rasmussen Jeffrey P, Vo Nhat-Thi, Sagasti Alvaro   Fish Scales Dictate the Pattern of Adult Skin Innervation and Vascularization Developmental cell, 2018; 46(3): 344-359.e4.
Madigan Cressida A, Cambier C J, Kelly-Scumpia Kindra M, Scumpia Philip O, Cheng Tan-Yun, Zailaa Joseph, Bloom Barry R, Moody D Branch, Smale Stephen T, Sagasti Alvaro, Modlin Robert L, Ramakrishnan Lalita   A Macrophage Response to Mycobacterium leprae Phenolic Glycolipid Initiates Nerve Damage in Leprosy Cell, 2017; 170(5): 973-985.e10.
Inaba Yasuko, Chauhan Vasudha, van Loon Aaron Paul, Choudhury Lamia Saiyara, Sagasti Alvaro   Keratins and the plakin family cytolinker proteins control the length of epithelial microridge protrusions eLife, 2020; 9: .
Jiang Nan, Rasmussen Jeffrey P, Clanton Joshua A, Rosenberg Marci F, Luedke Kory P, Cronan Mark R, Parker Edward D, Kim Hyeon-Jin, Vaughan Joshua C, Sagasti Alvaro, Parrish Jay Z   A conserved morphogenetic mechanism for epidermal ensheathment of nociceptive sensory neurites eLife, 2019; 8(9): R327-R329.
van Loon Aaron P, Erofeev Ivan S, Maryshev Ivan V, Goryachev Andrew B, Sagasti Alvaro   Cortical contraction drives the 3D patterning of epithelial cell surfaces The Journal of cell biology, 2020; 219(3): .
Julien Donald P, Chan Alex W, Barrios Joshua, Mathiaparanam Jaffna, Douglass Adam, Wolman Marc A, Sagasti Alvaro   Zebrafish expression reporters and mutants reveal that the IgSF cell adhesion molecule Dscamb is required for feeding and survival Journal of neurogenetics, 2018; 32(4): 336-352.
Cokus Shawn J, De La Torre Maricruz, Medina Eric F, Rasmussen Jeffrey P, Ramirez-Gutierrez Joselyn, Sagasti Alvaro, Wang Fang   Tissue-Specific Transcriptomes Reveal Gene Expression Trajectories in Two Maturing Skin Epithelial Layers in Zebrafish Embryos G3 (Bethesda, Md.), 2019; 9(10): 3439-3452.