The complete DNA sequence of the Dictyostelium discoideum genome will be determined over a five-year period at an average cost of 21 cents per base. The thirty-four million basepair sequence will be highly accurate (greater than 99.99 percent) and contain few gaps. The sequence data will be analyzed for gene-content, richly annotated, and immediately released to the public. These data will facilitate subsequent molecular analyses of gene function in this organism and will be indispensable for defining genes present in all eukaryotic organisms, including humans. A combined clone-mapping and shotgun-sequencing strategy will be employed to obtain complete sequences of Bacterial Artificial Chromosomes (BACs) carrying large segments (4 percent) of the genome. The shotgun strategy used will minimize redundant sequencing, and thus increase efficiency and lower costs. Gaps in the sequence will be filled by sequencing additional BAC clones and by sequencing selected clones from an independent library of Yeast Artificial Chromosomes (YACs), which have already been ordered along the Dictyostelium chromosomes and represent the genome with high fidelity. There are compelling reasons to sequencing the complete genome of Dictyostelium. Studies in over 150 laboratories world-wide have shown that these soil amoebae are an excellent system for the analysis of the molecular mechanisms of cell motility, signal transduction, cell-type differentiation and a host of developmental processes. As the total complement of genes is uncovered, tests of their function can proceed logically in the context of a rich knowledge-base in these areas. Detailed molecular descriptions of the functions of genes described in other species as well as """"""""pathfinder"""""""" genes can be worked out in the relatively simple setting of Dictyostelium cell physiology. As the functions for these genes are defined in Dictyostelium additional clues to their function in other species will be revealed. This will inevitably improve our ability to interpret the potential function of human genes, their roles in normal physiology and development, and may shed light the problems created by aberrant gene products in the pathogenesis of various diseases.

Agency
National Institute of Health (NIH)
Institute
Eunice Kennedy Shriver National Institute of Child Health & Human Development (NICHD)
Type
Research Project (R01)
Project #
5R01HD035925-02
Application #
2889435
Study Section
Special Emphasis Panel (ZRG2-MGN (02))
Program Officer
Moody, Sally Ann
Project Start
1998-09-21
Project End
2001-06-30
Budget Start
1999-07-01
Budget End
2000-06-30
Support Year
2
Fiscal Year
1999
Total Cost
Indirect Cost
Name
Baylor College of Medicine
Department
Biochemistry
Type
Schools of Medicine
DUNS #
074615394
City
Houston
State
TX
Country
United States
Zip Code
77030
Eichinger, L; Pachebat, J A; Glockner, G et al. (2005) The genome of the social amoeba Dictyostelium discoideum. Nature 435:43-57
Song, Jie; Xu, Qikai; Olsen, Rolf et al. (2005) Comparing the Dictyostelium and Entamoeba genomes reveals an ancient split in the Conosa lineage. PLoS Comput Biol 1:e71
Raisley, Brent; Zhang, Minghang; Hereld, Dale et al. (2004) A cAMP receptor-like G protein-coupled receptor with roles in growth regulation and development. Dev Biol 265:433-45
Sucgang, Richard; Chen, Guokai; Liu, Wen et al. (2003) Sequence and structure of the extrachromosomal palindrome encoding the ribosomal RNA genes in Dictyostelium. Nucleic Acids Res 31:2361-8