Barbara Wold | |
---|---|
Born | 1951 |
Alma mater | Arizona State University (Tempe), California Institute of Technology |
Scientific career | |
Fields | Developmental Biology and Genetics, Systems Biology |
Institutions | Beckman Institute, California Institute of Technology |
Thesis | Studies of structural gene transcripts in sea urchin embryos and adult tissues (1978) |
Doctoral advisor | Eric H. Davidson |
Doctoral students | Tracy Teal Ardem Patapoutian |
Barbara J. Wold is the Bren Professor of Molecular Biology, [1] the principal investigator of the Wold Lab [2] at the California Institute of Technology (Caltech) and the principal investigator of the Functional Genomics Resource Center at the Beckman Institute at Caltech. [3] Wold was director of the Beckman Institute at Caltech from 2001 to 2011. [4]
Barbara Wold graduated with a B. S. in zoology from Arizona State University (Tempe) in 1973. She was inspired by laboratory work with zoology professor Shelby Gerking and developmental biologist Jerry Justus, and lectures with professor emerita Kathleen Church. While at ASU, Wold became interested in understanding the informational code that regulates gene expression. [1] She also met her husband, geophysicist Lawrence "Larry" Burdick. [1]
Wold received a Ph.D. in molecular developmental biology from the California Institute of Technology (Caltech) in 1978, [5] studying genome structure and gene regulation during embryo development. [6] She was appointed as a postdoctoral research fellow at Columbia University College of Physicians and Surgeons in 1978. [5] There she developed methods for assaying cis-regulatory element function. [6]
In 1981, Wold returned to Caltech as an assistant professor in the Biology department. She was promoted to associate professor in 1988 and full professor in 1996, holding the position until 2002. She became Bren Professor of Molecular Biology as of 2003. [7]
Wold helped to found the L. K. Whittier Gene Expression Center at Caltech in 1999, with Stephen Quake and Mel Simon, collaborating with the Human Genome Project. [8] She has also been involved in establishing the Center for Biological Circuit Design at Caltech. [9] She has been an advisor to the National Institutes of Health and the Department of Energy in the area of genomics. [5] [10]
Wold was director of the Beckman Institute at Caltech from 2001 to 2011, succeeding founding director Harry B. Gray. [5] As of January 30, 2012, she was succeeded as director by David A. Tirrell. [4]
Barbara Wold has published more than sixty papers in the areas of developmental biology and genetics. [5] Throughout her career, Wold has focused on exploring the architecture and logic of gene regulatory networks, in an effort to understand the mechanisms that drive cell state transitions in the development and differentiation of individual cells. In particular, she has investigated the ways in which these differentiation mechanisms are encoded in DNA, and furthermore, how they are executed via transcription. [11]
Beginning with undifferentiated precursor cells, Wold and her lab have focused particularly on transitions from mesodermal cells in early development to fully developed skeletal muscle and cardiac muscle in animals, primarily through the use of mouse models. In addition, she is interested in the transitions in cell development which lead to tumorigenesis. [12]
Wold and her lab have used various techniques, [2] including genome-wide and proteome-wide assays, wet-bench genomic technology, and computational methods, many of which they have developed in conjunction with other researchers, to study skeletal muscle development, degeneration and regeneration. [12] She has also used such techniques as microarray gene expression analysis, global protein/DNA interaction measures, mass spectrometry-based proteomics, and comparative genomics. [12] In collaboration with others, her lab has also pioneered a modification of mass spectrometry and dual-affinity epitope tagging that enables efficient and accurate classification of multi-protein complexes. [12]
Much of Wold's recent work focuses on biological information processing, developing and using new techniques such as ultra-high-throughput DNA sequencing techniques [13] to computationally model the inputs and outputs of gene networks. She studies embryonic development and regeneration in vertebrates, examining transcriptional networks and using comparative genomics to model mouse, human and dog genomes. This work is leading to increased understanding of direct transcriptional regulation and of post-transcriptional and translational mechanisms and their mediation by microRNAs. [14] Wold's goal is a deep understanding of biological circuit design and the mechanisms of genetics and cell development. [9] To this end, Wold seeks to use her research to contribute to the development of the international reference transcriptome and regulatory element databases. [11]
Wold's lab has recently been concerned with human disease genomics. In particular, they are looking into diseases such as Alzheimer's, cancer, and musculoskeletal disorders. [11]
Gene expression is the process by which information from a gene is used in the synthesis of a functional gene product that enables it to produce end products, proteins or non-coding RNA, and ultimately affect a phenotype. These products are often proteins, but in non-protein-coding genes such as transfer RNA (tRNA) and small nuclear RNA (snRNA), the product is a functional non-coding RNA. The process of gene expression is used by all known life—eukaryotes, prokaryotes, and utilized by viruses—to generate the macromolecular machinery for life.
David Baltimore is an American biologist, university administrator, and 1975 Nobel laureate in Physiology or Medicine. He is a professor of biology at the California Institute of Technology (Caltech), where he served as president from 1997 to 2006. He founded the Whitehead Institute and directed it from 1982 to 1990. In 2008, he served as president of the American Association for the Advancement of Science in 2008.
In genetics, an enhancer is a short region of DNA that can be bound by proteins (activators) to increase the likelihood that transcription of a particular gene will occur. These proteins are usually referred to as transcription factors. Enhancers are cis-acting. They can be located up to 1 Mbp away from the gene, upstream or downstream from the start site. There are hundreds of thousands of enhancers in the human genome. They are found in both prokaryotes and eukaryotes.
Leroy "Lee" Edward Hood is an American biologist who has served on the faculties at the California Institute of Technology (Caltech) and the University of Washington. Hood has developed ground-breaking scientific instruments which made possible major advances in the biological sciences and the medical sciences. These include the first gas phase protein sequencer (1982), for determining the sequence of amino acids in a given protein; a DNA synthesizer (1983), to synthesize short sections of DNA; a peptide synthesizer (1984), to combine amino acids into longer peptides and short proteins; the first automated DNA sequencer (1986), to identify the order of nucleotides in DNA; ink-jet oligonucleotide technology for synthesizing DNA and nanostring technology for analyzing single molecules of DNA and RNA.
In molecular biology and genetics, transcriptional regulation is the means by which a cell regulates the conversion of DNA to RNA (transcription), thereby orchestrating gene activity. A single gene can be regulated in a range of ways, from altering the number of copies of RNA that are transcribed, to the temporal control of when the gene is transcribed. This control allows the cell or organism to respond to a variety of intra- and extracellular signals and thus mount a response. Some examples of this include producing the mRNA that encode enzymes to adapt to a change in a food source, producing the gene products involved in cell cycle specific activities, and producing the gene products responsible for cellular differentiation in multicellular eukaryotes, as studied in evolutionary developmental biology.
Functional genomics is a field of molecular biology that attempts to describe gene functions and interactions. Functional genomics make use of the vast data generated by genomic and transcriptomic projects. Functional genomics focuses on the dynamic aspects such as gene transcription, translation, regulation of gene expression and protein–protein interactions, as opposed to the static aspects of the genomic information such as DNA sequence or structures. A key characteristic of functional genomics studies is their genome-wide approach to these questions, generally involving high-throughput methods rather than a more traditional "candidate-gene" approach.
Tom Maniatis, is an American professor of molecular and cellular biology. He is a professor at Columbia University, and serves as the Scientific Director and CEO of the New York Genome Center.
The Encyclopedia of DNA Elements (ENCODE) is a public research project which aims "to build a comprehensive parts list of functional elements in the human genome."
In biology, the word gene has two meanings. The Mendelian gene is a basic unit of heredity. The molecular gene is a sequence of nucleotides in DNA, that is transcribed to produce a functional RNA. There are two types of molecular genes: protein-coding genes and non-coding genes.
Eric Harris Davidson was an American developmental biologist at the California Institute of Technology. Davidson was best known for his pioneering work on the role of gene regulation in evolution, on embryonic specification and for spearheading the effort to sequence the genome of the purple sea urchin, Strongylocentrotus purpuratus. He devoted a large part of his professional career to developing an understanding of embryogenesis at the genetic level. He wrote many academic works describing his work, including a textbook on early animal development.
Peter B. Dervan is the Bren Professor of Chemistry at the California Institute of Technology. The primary focus of his research is the development and study of small organic molecules that can sequence-specifically recognize DNA, a field in which he is an internationally recognized authority. The most important of these small molecules are pyrrole–imidazole polyamides. Dervan is credited with influencing "the course of research in organic chemistry through his studies at the interface of chemistry and biology" as a result of his work on "the chemical principles involved in sequence-specific recognition of double helical DNA". He is the recipient of many awards, including the National Medal of Science (2006).
Barbara J. Meyer is a biologist and genetist, noted for her pioneering research on lambda phage, a virus that infects bacteria; discovery of the master control gene involved in sex determination; and studies of gene regulation, particularly dosage compensation. Meyer's work has revealed mechanisms of sex determination and dosage compensation—that balance X-chromosome gene expression between the sexes in Caenorhabditis elegans that continue to serve as the foundation of diverse areas of study on chromosome structure and function today.
Epigenomics is the study of the complete set of epigenetic modifications on the genetic material of a cell, known as the epigenome. The field is analogous to genomics and proteomics, which are the study of the genome and proteome of a cell. Epigenetic modifications are reversible modifications on a cell's DNA or histones that affect gene expression without altering the DNA sequence. Epigenomic maintenance is a continuous process and plays an important role in stability of eukaryotic genomes by taking part in crucial biological mechanisms like DNA repair. Plant flavones are said to be inhibiting epigenomic marks that cause cancers. Two of the most characterized epigenetic modifications are DNA methylation and histone modification. Epigenetic modifications play an important role in gene expression and regulation, and are involved in numerous cellular processes such as in differentiation/development and tumorigenesis. The study of epigenetics on a global level has been made possible only recently through the adaptation of genomic high-throughput assays.
Albert Erives is a developmental geneticist who studies transcriptional enhancers underlying animal development and diseases of development (cancers). Erives also proposed the pacRNA model for the dual origin of the genetic code and universal homochirality. He is known for work at the intersection of genetics, evolution, developmental biology, and gene regulation. He has worked at the California Institute of Technology, University of California, Berkeley, and Dartmouth College, and is an associate professor at the University of Iowa.
Marianne Bronner is a developmental biologist who currently serves as Edward B. Lewis Professor of Biology and an executive officer for Neurobiology at the California Institute of Technology. Her most notable work includes her research on the neural crest. Bronner's research focuses on studying the cellular events behind the migration, differentiation, and formation of neural crest cells. She currently directs her own laboratory at the California Institute of Technology called the Bronner Laboratory, and she has authored over 400 articles in her field.
Roger Brent is an American biologist known for his work on gene regulation and systems biology. He studies the quantitative behaviors of cell signaling systems and the origins and consequences of variation in them. He is Full Member in the Division of Basic Sciences at the Fred Hutchinson Cancer Research Center and an Affiliate Professor of Genome Sciences at the University of Washington.
The Beckman Institute at Caltech is a multi-disciplinary center for research in the chemical and biological sciences, located at and partnering with the California Institute of Technology (Caltech) in Pasadena, California, United States.
Manolis Kellis is a professor of Computer Science and Computational Biology at the Massachusetts Institute of Technology (MIT) and a member of the Broad Institute of MIT and Harvard. He is the head of the Computational Biology Group at MIT and is a Principal Investigator in the Computer Science and Artificial Intelligence Lab (CSAIL) at MIT.
Ellen V. Rothenberg is an American biologist who is an Edward B. Lewis Professor of Biology at the California Institute of Technology. She investigates the molecular mechanisms that underpin lineage choice. She is an elected fellow of the American Association for the Advancement of Science, American Academy of Arts and Sciences and the National Academy of Sciences.
Eileen E. M. Furlong is an Irish molecular biologist working in the fields of transcription, chromatin biology, developmental biology and genomics. She is known for her work in understanding how the genome is regulated, in particular to how developmental enhancers function, how they interact within three dimensional chromatin topologies and how they drive cell fate decisions during embryogenesis. She is Head of the Department of Genome Biology at the European Molecular Biology Laboratory (EMBL). Furlong was elected a member of the European Molecular Biology Organization (EMBO) in 2013, the Academia Europaea in 2016 and to EMBO’s research council in 2018.