Genome History
Science v.291, n.5507 16fe01
1953
Watson and Crick |
(April) James Watson and Francis
Crick discover the double helical structure of DNA
(Nature).
1972
(October) Paul Berg and co-workers create
the first recombinant DNA molecule (PNAS).
1977
Allan Maxam and Walter Gilbert
(pictured) at Harvard University and Frederick
Sanger at the U.K. Medical Research Council (MRC)
independently develop methods for sequencing DNA (PNAS,
February; PNAS, December).
1980
(May) David Botstein of the Massachusetts
Institute of Technology, Ronald Davis of
Stanford University, and Mark Skolnick and Ray
White of the University of Utah propose a method to
map the entire human genome based on RFLPs
(American Journal of Human Genetics).
1982
Akiyoshi Wada (pictured), now at RIKEN in
Japan, proposes automated sequencing and gets support to
build robots with help from Hitachi.
1984
(May) Charles Cantor and David
Schwartz of Columbia University develop pulsed
field electrophoresis (Cell).
(July) MRC scientists decipher the complete DNA sequence of
the Epstein-Barr virus, 170 kb (Nature).
1985
(May) Robert Sinsheimer (pictured) hosts a
meeting at the University of California (UC), Santa Cruz, to
discuss the feasibility of sequencing the human genome.
(December) Kary Mullis and colleagues at
Cetus Corp. develop PCR,
a technique to replicate vast amounts of DNA (Science).
1986
(February) Sydney Brenner of MRC urges the
European Union to undertake a concerted program to map and
sequence the human genome; Brenner also starts a small
genome initiative at MRC.
(March) The U.S. Department of Energy (DOE) hosts a meeting
in Santa Fe, New Mexico, to discuss plans to sequence the
human genome.
(March) Renato Dulbecco of the Salk
Institute promotes sequencing the human genome in a paper (Science).
(June) Merits of a human genome project are hotly debated at
a meeting at Cold Spring Harbor Laboratory in New York
state, "The Molecular Biology of Homo sapiens."
(pictured)
(June) Leroy Hood (pictured) and Lloyd
Smith of the California Institute of Technology
(Caltech) and colleagues announce the first automated DNA
sequencing machine (Nature).
(September) Charles DeLisi begins genome
studies at DOE, reallocating $5.3 million from the fiscal
year 1987 budget.
1987
(February) Walter Gilbert resigns from the
U.S. National Research Council (NRC) genome panel and
announces plans to start Genome Corp., with the goal of
sequencing and copyrighting the human genome and selling
data for profit.
(April) An advisory panel suggests that DOE should spend $1
billion on mapping and sequencing the human genome over the
next 7 years-and that DOE should lead the U.S. effort. DOE's
Human Genome Initiative begins.
(May) David Burke, Maynard Olson,
and George Carle of Washington University
in St. Louis develop YACs
(left) for cloning, increasing insert size 10-fold (Science).
(October) Helen Donis-Keller and colleagues
at Collaborative Research Inc. publish the "first"
genetic map with 403 markers, sparking a fight over credit
and priority (Cell).
(October) DuPont scientists develop a system for rapid DNA
sequencing with fluorescent chain-terminating
dideoxynucleotides (Science).
Applied Biosystems Inc. puts the first automated sequencing
machine, based on Hood's technology, on the market.
1988
(February) In a pivotal report, the NRC endorses the Human
Genome Project (HGP), calling for a phased approach and a
rapid scale-up to $200 million a year of new money.
(March) Prompted by advisers at a meeting in Reston,
Virginia, James Wyngaarden, then director
of the National Institutes of Health (NIH), decides that the
agency should be a major player in the HGP, effectively
seizing the lead from DOE.
(June) The first annual genome meeting is held at Cold
Spring Harbor Laboratory.
(September) NIH establishes the Office of Human Genome
Research and snags Watson (pictured) as its
head. Watson declares that 3% of the genome budget should be
devoted to studies of social and ethical issues.
(October) NIH and DOE sign a memorandum of understanding and
agree to collaborate on the HGP.
1989
(January) Norton Zinder of Rockefeller
University chairs the first program advisory committee
meeting for the HGP.
(September) Olson, Hood, Botstein,
and Cantor outline a new mapping strategy,
using STSs (Science).
(September) DOE and NIH start a joint committee on the
ethical, legal, and social implications of the HGP.
(October) NIH office is elevated to the National Center for
Human Genome Research (NCHGR), with grant-awarding
authority.
1990
Three groups develop capillary electrophoresis (left), one
team led by Lloyd Smith (Nucleic Acids
Research, August), the second by Barry Karger
(Analytical Chemistry, January), and the third by Norman
Dovichi (Journal of Chromatography,
September).
(April) NIH and DOE publish a 5-year plan. Goals include a
complete genetic map, a physical map with markers every 100
kb, and sequencing of an aggregate of 20 Mb of DNA in model
organisms by 2005.
(August) NIH begins large-scale sequencing trials on four
model organisms: Mycoplasma capricolum, Escherichia
coli (left, pink), Caenorhabditis elegans
(left, rainbow), and Saccharomyces cerevisiae
(left, ovals). Each research group agrees to sequence 3 Mb
at 75 cents a base within 3 years.
(October) NIH and DOE restart the clock, declaring 1 October
the official beginning of the HGP.
(October) David Lipman, Eugene
Myers, and colleagues at the National Center for
Biotechnology Information (NCBI) publish the BLAST
algorithm for aligning sequences (Journal of Molecular
Biology).
1991
(June) NIH biologist J. Craig Venter
announces a strategy to find expressed genes, using ESTs
(Science). A fight erupts at a congressional
hearing 1 month later, when Venter reveals
that NIH is filing patent applications on thousands of these
partial genes.
(October) The Japanese rice genome sequencing effort begins.
(December) Edward Uberbacher of Oak Ridge
National Laboratory in Tennessee develops GRAIL, the first
of many gene-finding programs (PNAS).
1992
(April) After a dispute with then-NIH director Bernadine
Healy over patenting partial genes, Watson
resigns as head of NCHGR.
(June) Venter leaves NIH to set up The
Institute for Genomic Research (TIGR), a nonprofit in
Rockville, Maryland. William Haseltine
heads its sister company, Human Genome Sciences, to
commercialize TIGR products.
(July) Britain's Wellcome Trust enters the HGP with $95
million.
(September) Mel Simon of Caltech and
colleagues develop BACs for cloning (PNAS).
(October) U.S. and French teams complete the first physical
maps of chromosomes: David Page of the
Whitehead Institute and colleagues (pictured) map the Y
chromosome (Science); Daniel Cohen
of the Centre d'Etude du Polymorphisme Humain (CEPH) and Généthon
and colleagues map chromosome 21 (Nature).
(December) After lengthy debate, NIH and DOE release
guidelines on sharing data and resources, encouraging rapid
sharing and enabling researchers to keep data private for 6
months.
U.S. and French teams complete genetic maps of mouse and
human: mouse, average marker spacing 4.3 cM,
Eric Lander and colleagues at Whitehead (Genetics,
June); human, average marker spacing 5 cM, Jean
Weissenbach and colleagues at CEPH (Nature,
October).
1993
(April) Francis Collins of the University
of Michigan is named director of NCHGR.
(October) NIH and DOE publish a revised plan for 1993-98.
The goals include sequencing 80 Mb of DNA by the end of 1998
and completing the human genome by 2005.
(October) The Wellcome Trust and MRC open the Sanger Centre
at Hinxton Hall, south of Cambridge, U.K. Led by John
Sulston (pictured), the center becomes one of the
major sequencing labs in the international consortium.
(October) The GenBank database officially moves from Los
Alamos to NCBI, ending NIH's and DOE's tussle over control.
1994
(September) Jeffrey Murray of the
University of Iowa, Cohen of Généthon,
and colleagues publish a complete genetic linkage map of the
human genome, with an average marker spacing of 0.7 cM (Science).
1995
(May to August) Richard Mathies and
colleagues at UC Berkeley and Amersham develop improved
sequencing dyes (PNAS, May); Michael Reeve
and Carl Fuller at Amersham develop
thermostable polymerase (Nature, August).
(July) Venter and Claire Fraser
of TIGR and Hamilton Smith of Johns Hopkins
publish the first sequence of a free-living organism, Haemophilus
influenzae, 1.8 Mb (Science).
(September) The Japanese government funds several sequencing
groups for a total of $15.9 million over 5 years: Tokai
University, University of Tokyo, and Keio University.
(October) Patrick Brown of Stanford and
colleagues publish first paper using a printed glass
microarray of complementary DNA (cDNA) probes (Science).
(December) Researchers at Whitehead and Généthon (led by Lander
and Thomas Hudson at Whitehead) publish a
physical map of the human genome containing 15,000 markers (Science).
1996
(February) At a meeting in Bermuda funded by the Wellcome
Trust, international HGP partners agree to release sequence
data into public databases within 24 hours.
(April) NIH funds six groups to attempt large-scale
sequencing of the human genome.
(April) Affymetrix makes DNA chips commercially available.
(September) DOE initiates six pilot projects, funded at $5
million total, to sequence the ends of BAC clones.
(October) An international consortium publicly releases the
complete genome sequence of the yeast S. cerevisiae
(Science).
(November) Yoshihide Hayashizaki's group at
RIKEN completes the first set of full-length mouse cDNAs.
1997
(January) NCHGR is promoted to the National Human Genome
Research Institute; DOE creates the Joint Genome Institute.
(September) Fred Blattner, Guy
Plunkett, and University of Wisconsin, Madison,
colleagues complete the DNA sequence of E. coli, 5
Mb (Science).
(September) Molecular Dynamics introduces the MegaBACE,
a capillary sequencing machine.
1998
(January) NIH announces a new project to find SNPs.
(February) Representatives of Japan, the U.S., the E.U.,
China, and South Korea meet in Tsukuba, Japan, to establish
guidelines for an international collaboration to sequence
the rice genome.
(March) Phil Green (pictured) and Brent
Ewing of Washington University and colleagues
publish a program called phred for automatically
interpreting sequencer data (Genetic Research).
Both phred and its sister program phrap (used for assembling
sequences) had been in wide use since 1995.
(May) PE Biosystems Inc. introduces the PE Prism 3700
capillary sequencing machine.
(May) Venter announces a new company named
Celera and declares that it will sequence the human genome
within 3 years for $300 million.
(May) In response, the Wellcome Trust doubles its support
for the HGP to $330 million, taking on responsibility for
one-third of the sequencing.
(October) NIH and DOE throw HGP into overdrive with a new
goal of creating a "working draft" of the human
genome by 2001, and they move the completion date for the
finished draft from 2005 to 2003.
(December) Sulston of the Sanger Centre and
Robert Waterston of Washington University
and colleagues complete the genomic sequence of C.
elegans (Science).
1999
(March) NIH again moves up the completion date for the rough
draft, to spring 2000. Large-scale sequencing efforts are
concentrated in centers at Whitehead, Washington University,
Baylor, Sanger, and DOE's Joint Genome Institute.
(April) Ten companies and the Wellcome Trust launch the SNP
consortium, with plans to publicly release data quarterly.
(September) NIH launches a project to sequence the mouse
genome, devoting $130 million over 3 years.
(December) British, Japanese, and U.S. researchers complete
the first sequence of a human chromosome, number 22 (Nature).
2000
(March) Celera and academic collaborators sequence the
180-Mb genome of the fruit fly Drosophila melanogaster
(left), the largest genome yet sequenced and a validation of
Venter's controversial whole-genome shotgun
method (Science).
(March) Because of disagreement over a data-release policy,
plans for HGP and Celera to collaborate disintegrate amid
considerable sniping.
(May) HGP consortium led by German and Japanese researchers
publishes the complete sequence of chromosome 21 (Nature).
(June) At a White House ceremony, HGP and Celera jointly
announce working drafts of the human genome sequence,
declare their feud at an end, and promise simultaneous
publication.
(October) DOE and MRC launch a collaborative project to
sequence the genome of the puffer fish, Fugu rubripes
(left), by March 2001.
(December) An international consortium completes the
sequencing of the first plant, Arabidopsis thaliana
(left), 125 Mb.
(December) HGP and Celera's plans for joint publication in Science
collapse; HGP sends its paper to Nature.
2001
(February) The HGP consortium publishes its working draft in
Nature (15 February), and Celera publishes its
draft in Science (16 February).
source: http://www.sciencemag.org/genome2001/1195.html 13feb01 from collection at http://www.sciencemag.org/cgi/collection/genetics
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