The long-range goal of this project is to understand parameters which determine spatial and functional organization of DNA in the nucleus. Specifically, the work will identify chromosomal DNA sites which are anchored to immobile objects in yeast Saccharomyces cerevisiae. DNA immobilization by specific DNA sequences may represent a fundamental unit of chromosome architecture; DNA anchors may segregate chromosomal DNA into independent structural domains for DNA packaging, regulated gene expression and positioning within the nucleus. DNA anchoring sequences and associated proteins will be characterized using a newly developed molecular biological technique. The approach employs site specific recombination in vivo to generate well-defined DNA rings which contain a single promoter and a DNA fragment to be tested. Transcription of anchored DNA rings ina yeast topoisomerase mutants leads to diagnostic changes in DNA topology, in accordance with the twin domain model of transcriptional supercoiling. models of DNA organization based on analyses of biochemically manipulated chromosomes, termed nuclear scaffold, argue that DNA is arranged into loops with specific DNA segments anchoring the bases of the loops to an organizational framework. The excision methodology will be used to investigate whether sequences which bind yeast scaffold preparations function as DNA anchors in vivo. Scaffold attachment regions (SARs) to be examined include chromosomal components such as telomeres, silencers, centromeres and origins of replication. DNA anchor formation. The cell- cycle dependent anchoring of centromeres and replication origins will be determined in synchronized cell cultures. A selection system will be developed to isolate sequences with DNA anchoring activity from libraries of the sequenced yeast Chromosome III. The DNA loop structure of specific chromosomal regions will be determined by mapping the DNA anchoring elements which reside within the regions. The influence of genomic DNA anchors on plasmid partitioning and gene expression will be examined.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
1R01GM051402-01A1
Application #
2189905
Study Section
Molecular Cytology Study Section (CTY)
Project Start
1994-09-12
Project End
1999-06-30
Budget Start
1995-07-01
Budget End
1996-06-30
Support Year
1
Fiscal Year
1995
Total Cost
Indirect Cost
Name
University of Medicine & Dentistry of NJ
Department
Pharmacology
Type
Schools of Medicine
DUNS #
622146454
City
Piscataway
State
NJ
Country
United States
Zip Code
08854
Gartenberg, Marc R; Smith, Jeffrey S (2016) The Nuts and Bolts of Transcriptionally Silent Chromatin in Saccharomyces cerevisiae. Genetics 203:1563-99
Chou, Chia-Ching; Patel, Michael T; Gartenberg, Marc R (2015) A series of conditional shuttle vectors for targeted genomic integration in budding yeast. FEMS Yeast Res 15:
Chen, Miao; Gartenberg, Marc R (2014) Coordination of tRNA transcription with export at nuclear pore complexes in budding yeast. Genes Dev 28:959-70
Fox, Catherine A; Gartenberg, Marc R (2012) Palmitoylation in the nucleus: a little fat around the edges. Nucleus 3:251-5
Gartenberg, Marc R (2012) Generation of DNA circles in yeast by inducible site-specific recombination. Methods Mol Biol 833:103-13
Ruben, Giulia J; Kirkland, Jacob G; MacDonough, Tracy et al. (2011) Nucleoporin mediated nuclear positioning and silencing of HMR. PLoS One 6:e21923
Wu, Ching-Shyi; Chen, Yu-Fan; Gartenberg, Marc R (2011) Targeted sister chromatid cohesion by Sir2. PLoS Genet 7:e1002000
Park, Sookhee; Patterson, Erin E; Cobb, Jenel et al. (2011) Palmitoylation controls the dynamics of budding-yeast heterochromatin via the telomere-binding protein Rif1. Proc Natl Acad Sci U S A 108:14572-7
Gartenberg, Marc R (2009) Life on the edge: telomeres and persistent DNA breaks converge at the nuclear periphery. Genes Dev 23:1027-31
Gartenberg, Marc (2009) Heterochromatin and the cohesion of sister chromatids. Chromosome Res 17:229-38

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