Cold Spring Harbor Laboratory (CSHL) is a private, non-profit institution with research programs focusing on cancer, neuroscience, plant genetics, genomics, and quantitative biology.
It is one of 68 institutions supported by the Cancer Centers Program of the U.S. National Cancer Institute (NCI) and has been an NCI-designated Cancer Center since 1987. The Laboratory is one of a handful of institutions that played a central role in the development of molecular genetics and molecular biology.
It has been home to eight scientists who have been awarded the Nobel Prize in Physiology or Medicine. CSHL is ranked among the leading basic research institutions in the world in molecular biology and genetics. The Laboratory is led by Bruce Stillman, a biochemist and cancer researcher.
Since its inception in 1890, the institution's campus on the North Shore of Long Island has also been a center of biology education. Current CSHL educational programs serve professional scientists, doctoral students in biology, teachers of biology in the K-12 system, and students from the elementary grades through high school. In the past 10 years CSHL conferences & courses have drawn over 81,000 scientists and students to the main campus. For this reason, many scientists consider CSHL a "crossroads of biological science." Since 2009 CSHL has partnered with the Suzhou Industrial Park in Suzhou, China to create Cold Spring Harbor Asia which annually draws some 3,000 scientists to its meetings and courses.
In 2015, CSHL announced a strategic affiliation with the nearby Northwell Health to advance cancer therapeutics research, develop a new clinical cancer research unit at Northwell Health in Lake Success, NY, to support early-phase clinical studies of new cancer therapies, and recruit and train more clinician-scientists in oncology.
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Research programs
Research staff in CSHL's 52 laboratories numbers over 600, including postdoctoral researchers; an additional 125 graduate students and 500 administrative and support personnel bring the total number of employees to over 1,200.
Cell biology and genomics
RNA interference (RNAi) and small-RNA biology; DNA replication; RNA splicing; signal transduction; genome structure; non-coding RNAs; deep sequencing; single-cell sequencing and analytics; chromatin dynamics; structural biology; advanced proteomics; mass spectrometry; advanced microscopy.
Cancer research
Principal cancer types under study: breast, prostate, blood (leukemia, lymphoma); melanoma; liver; ovarian and cervical; lung; brain; pancreas. Research foci: drug resistance; cancer genomics; tumor microenvironment; growth control in mammalian cells; transcriptional and post-transcriptional gene regulation.
Neuroscience
Stanley Institute for Cognitive Genomics employs deep sequencing and other tools to study genetics underlying schizophrenia, bipolar disorder, and major depression. Swartz Center for the Neural Mechanisms of Cognition studies cognition in the normal brain as a baseline for understanding dysfunction in psychiatric and neurodegenerative disorders. Other research foci: autism genetics; mapping of the mammalian brain; neural correlates of decision making.
Plant genetics
Plant genome sequencing; epigenetics and stem cell fate; stem cell signaling; using genetic insights to increase yield of staple crops, e.g., maize, rice, wheat; increase fruit yield in flowering plants, e.g., tomato. Other initiatives: genetics of aquatic plants for biofuel development; lead role in building National Science Foundation's iPlant cyberinfrastructure.
Simons Center for Quantitative Biology
Genome assembly and validation; mathematical modeling and algorithm development; population genetics; applied statistical and machine learning; biomedical text-mining; computational genomics; cloud computing and Big Data.
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Educational programs
In addition to its research mission, CSHL has a broad educational mission. The Watson School of Biological Sciences (WSBS), established in 1998, awards the Ph.D. degree and fully funds the research program of every student. Students are challenged to obtain their doctoral degree in 4-5 years. The Undergraduate Research Program (URP) for gifted college students (established in 1959), and the Partners for the Future Program for advanced high school students (established in 1990) are now hosted at the WSBS.
The CSHL Meetings & Courses Program brings over 8,500 scientists from around the world to Cold Spring Harbor annually to share research results - mostly unpublished--in 60 meetings, most held biannually; and to learn new technologies in 30 to 35 professional courses, most offered annually. The Cold Spring Harbor Symposium series, held every year since 1933 with the exception of three years during the Second World War, has been a forum for researchers in genetics, genomics, neuroscience and plant biology. At the Banbury Center, about 25-30 discussion-style meetings are held yearly for a limited number of invited participants. As of 2016 a two-week course at CSHL costs between $3,700 and $4,700 per student and a three-day conferences cost about $1,000 per attendee.
The DNA Learning Center (DNALC), founded in 1988, was among the early pioneers in developing hands-on genetics lab experiences for middle and high school students. In 2013, 31,000 students on Long Island and New York City were taught genetics labs at the DNALC and satellite facilities in New York. Over 9,000 high school biology teachers have participated in DNALC teacher-training programs.
The Cold Spring Harbor Laboratory Press has established a program consisting of seven journals, 190 books, laboratory manuals and protocols, and online services for research preprints.
Funding
In 2015, CSHL had an operating budget of $150 million, over $100 million of which was spent on research. Half of the research budget was devoted to cancer; 25% to neuroscience; 15% to genomics and quantitative biology; and 10% to plant genetics. The sources of research funding in 2015 were: 34% Federal (primarily National Institutes of Health and National Science Foundation); 26% auxiliary activities; 22% private philanthropy; 10% endowment; 3% corporate.
Founding and early years
The institution took root as The Biological Laboratory in 1890, a summer program for the education of college and high school teachers studying zoology, botany, comparative anatomy and nature. The program began as an initiative of Eugene G. Blackford and Franklin Hooper, director of the Brooklyn Institute of Arts and Sciences, the founding institution of The Brooklyn Museum. In 1904, the Carnegie Institution of Washington established the Station for Experimental Evolution at Cold Spring Harbor on an adjacent parcel. In 1921, the station was reorganized as the Carnegie Institution Department of Genetics.
Between 1910 and 1939, the laboratory was the base of the Eugenics Record Office of biologist Charles B. Davenport and his assistant Harry H. Laughlin, two prominent American eugenicists of the period. Davenport was director of the Carnegie Station from its inception until his retirement in 1934. In 1935 the Carnegie Institution sent a team to review the ERO's work, and as a result the ERO was ordered to stop all work. In 1939 the Institution withdrew funding for the ERO entirely, leading to its closure. The ERO's reports, articles, charts, and pedigrees were considered scientific facts in their day, but have since been discredited. However, its closure came 15 years after its findings were incorporated into the National Origins Act (Immigration Act of 1924), which severely reduced the number of immigrants to America from southern and eastern Europe who, Harry Laughlin testified, were racially inferior to the Nordic immigrants from England and Germany. Charles Davenport was also the founder and the first director of the International Federation of Eugenics Organizations in 1925. Today, Cold Spring Harbor Laboratory maintains the full historical records, communications and artifacts of the ERO for historical, teaching and research purposes. The documents are housed in a campus archive and can be accessed online and in a series of multimedia websites.
Carnegie Institution scientists at Cold Spring Harbor made many contributions to genetics and medicine. In 1908 George H. Shull discovered hybrid corn and the genetic principle behind it called heterosis, or "hybrid vigor." This would become the foundation of modern agricultural genetics. Clarence C. Little in 1916 was among the first scientists to demonstrate a genetic component of cancer. E. Carleton MacDowell in 1928 discovered a strain of mouse called C58 that developed spontaneous leukemia - an early mouse model of cancer. In 1933, Oscar Riddle isolated prolactin, the milk secretion hormone and Wilbur Swingle participated in the discovery of adrenocortical hormone, used to treat Addison's disease.
CSHL since 1940
Milislav Demerec was named director of the Laboratory in 1941. Demerec shifted the Laboratory's research focus to the genetics of microbes, thus setting investigators on a course to study the biochemical function of the gene. During World War Two, Demerec directed efforts at Cold Spring Harbor that resulted in major increases in penicillin production.
Beginning in 1941, and annually from 1945, three of the seminal figures of molecular genetics convened summer meetings at Cold Spring Harbor of what they called the Phage Group. Salvador Luria, of Indiana University; Max Delbrück, then of Vanderbilt University; and Alfred Hershey, then of Washington University, St. Louis, sought to discover the nature of genes through study of viruses called bacteriophages that infect bacteria.
- In 1945, Delbrück's famous Phage Course was taught for the first time, inspiring, among others, a young James D. Watson; it was repeated for many years after. CSH Symposia important in the cross-fertilization of ideas among molecular biology's pioneers were held in 1951, 1953, 1956, 1961, 1963, and 1966.
- At the CSH Symposium in summer 1953, Watson made the first public presentation of DNA's double-helix structure.
Nobel Prize winners who have worked at Cold Spring Harbor
- In 1944 Barbara McClintock discovered transposons ("jumping genes"), for which she received a Nobel Prize in 1983.
- In 1952 the "Waring blender experiments" of Alfred Hershey and Martha Chase confirmed DNA as the genetic material. Hershey shared a Nobel Prize with Salvador Luria and Max Delbrück in 1969, "for their discoveries concerning the replication mechanism and the genetic structure of viruses."
- James D. Watson, CSHL Director from 1968 to 1993, shared a Nobel Prize with Francis Crick and Maurice Wilkins in 1962 for their discovery of the double helix structure of DNA.
- Richard J. Roberts and Phillip A. Sharp shared a Nobel in 1993 for the discovery of discontinuous, or "split" genes, which revealed the RNA splicing mechanism.
- Carol Greider, who in 1992 discovered a relationship between cellular aging and damage to the ends of chromosomes, called telomeres, shared a Nobel Prize in 2009 with Elizabeth Blackburn and Jack W. Szostak for their work on telomere biology.
Contemporary research at CSHL
- In 1973, Richard J. Roberts begins development and dissemination of a large library of restriction enzymes, basic tools for molecular biology;
- In 1981 Michael Wigler co-discovers H-RAS, the first human cancer-causing gene, or oncogene;
- In 1988 Ed Harlow demonstrates that cancer-causing and cancer-preventing genes (oncogenes and tumor-suppressor genes) interact;
- In 1994, Bruce Stillman reconstitutes DNA replication in a test tube;
- In 2002, Gregory Hannon's team develops technology to generate libraries of short-hairpin RNAs (shRNAs), giving researchers the ability to switch genes on and off in living cells;
- In 2004, Wigler and Jonathan Sebat discover that enhancements and deletions of genetic material called copy number variations are common across the human population;
- In 2007, Wigler and Sebat discover that spontaneous or de novo mutations are found in people with autism;
- In 2007, Hannon, Emily Hodges, Z. Xuan and W. Richard McCombie develop technology to sequence the exome, the small subset of protein-coding genes within the much larger genome--now a mainstay of identifying genetic mutations in disease;
- In 2011, Wigler, James Hicks and Nick Navin perform the first genomic profile of single cancer cells from a patient's tumor;
- In 2011, Christopher Vakoc discovers an important new drug target, BRD4, for a lethal form of Acute Myelogenous Leukemia (AML);
- In 2014, Phase 3 trials begin for drug to treat spinal muscular atrophy (SMA), a neurodegenerative disease, based on Adrian Krainer's insights into alternative splicing.
- In 2014, Zachary Lippman publishes toolkit of gene variations in flowering plants, allowing breeders to maximize yield of tomato and other crops.
CSHL leadership
In 1962, the Department of Genetics, no longer supported by the Carnegie Institution of Washington, formally merged with the Biological Laboratory to form the Cold Spring Harbor Laboratory of Quantitative Biology. In 1970, the name was simplified to Cold Spring Harbor Laboratory.
James D. Watson served as the Laboratory's director and president for 35 years. Upon taking charge in 1968, he focused the Laboratory on cancer research, creating a tumor virus group and successfully obtaining federal funds for an expansion of cancer research capabilities. Watson placed CSHL on a firm financial footing. Inspired by his Nobel collaborator, Francis Crick, Watson initiated a major push to scale-up CSHL research on the brain and psychiatric disorders, beginning in the late 1980s. In 1990, work was completed on the Arnold and Mabel Beckman Laboratory, and the Marks Neuroscience Building was opened in 1999. In 1994, Watson ceased being director of the Laboratory and assumed the title of president. In 2004 he was named chancellor, a position he held until October 2007, when he retired at the age of 79 after views attributed to him on race and intelligence appeared in the British press. He is now chancellor emeritus.
Since 1994 biochemist and cancer biologist Bruce Stillman has led the Laboratory as director, and since 2003 as president. Stillman, a member of the National Academy of Sciences and a Fellow of the Royal Society, also continues to run a basic research lab, devoted to the study of DNA replication and chromosome maintenance. Stillman is credited with the 1991 discovery and elucidation of the mechanism of the Origin Recognition Complex (ORC), a highly conserved protein complex that recognizes and binds to specific DNA sequences, marking starting points for replication of the entire genome.
Stillman has presided over a major expansion of the Laboratory, its size growing threefold since he became director. With construction completed on six linked laboratory buildings on the Hillside Campus in 2009, CSHL added much-needed new laboratory space for cancer and neuroscience research, as well as space for a new program on quantitative biology to bring experts in mathematics, computer science, statistics, and physics to problems in biology.
Source of the article : Wikipedia
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