The long-term goal of this research is to understand the relationship between structure and function in the cell nucleus. We will concentrate on somatic and germ cells of Drosophila and on the giant nucleus or germinal vesicle (GV) of Xenopus oocytes. Chromosomes are the most prominent components of nuclei, but most nuclei also contain 3 other structures: nucleoli, Cajal bodies (CBs), and speckles (interchromatin granule clusters). The functions of the chromosomes and nucleoli are well understood, but the functions of CBs and speckles are much less clear. There is increasing evidence that parts of the RNA processing machinery of the nucleus are assembled in CBs before storage in the speckles and eventual transport to the chromosomes. We have proposed that CBs are also sites for assembly of parts of the transcription machinery itself. We will test this model by examining the newly-identified Drosophila CBs and by screening for Drosophila mutations that affect CB structure and function. We will look for specific assembly processes in CBs of Drosophila and Xenopus oocyte, and we will examine the movement of macromolecules between CBs, speckles, and the nucleoplasm. We will also study details of individual genes and their transcripts on the loops of the lampbrush chromosomes by fluorescent in situ hybridization and immunofluorescent staining. These techniques allow one to examine how individual transcription units are organized and how nascent transcripts are modified while they remain associated with the chromosome. We will use the same techniques to produce physical maps of the lampbrush chromosomes of Xenopus tropicalis, using genomic probes generated by the Xenopus tropicalis Genome Project. These studies will provide insight into the structure and function of the major nuclear organelles and how they interact during transcription and processing of nuclear RNA.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
5R01GM033397-24
Application #
7432505
Study Section
Special Emphasis Panel (ZRG1-NDT (01))
Program Officer
Carter, Anthony D
Project Start
1983-09-01
Project End
2009-06-30
Budget Start
2008-07-01
Budget End
2009-06-30
Support Year
24
Fiscal Year
2008
Total Cost
$458,191
Indirect Cost
Name
Carnegie Institution of Washington, D.C.
Department
Type
DUNS #
072641707
City
Washington
State
DC
Country
United States
Zip Code
20005
Talhouarne, Gaëlle J S; Gall, Joseph G (2018) 7SL RNA in vertebrate red blood cells. RNA 24:908-914
Gall, Joseph G (2018) Herbert Macgregor (1933-2018). Chromosome Res :
Talhouarne, Gaëlle J S; Gall, Joseph G (2018) Lariat intronic RNAs in the cytoplasm of vertebrate cells. Proc Natl Acad Sci U S A 115:E7970-E7977
Deryusheva, Svetlana; Gall, Joseph G (2018) Orchestrated positioning of post-transcriptional modifications at the branch point recognition region of U2 snRNA. RNA 24:30-42
Deryusheva, Svetlana; Gall, Joseph G (2017) Dual nature of pseudouridylation in U2 snRNA: Pus1p-dependent and Pus1p-independent activities in yeasts and higher eukaryotes. RNA 23:1060-1067
Shi, Kevin Y; Mori, Eiichiro; Nizami, Zehra F et al. (2017) Toxic PRn poly-dipeptides encoded by the C9orf72 repeat expansion block nuclear import and export. Proc Natl Acad Sci U S A 114:E1111-E1117
Gall, Joseph G; Nizami, Zehra F (2016) Isolation of Giant Lampbrush Chromosomes from Living Oocytes of Frogs and Salamanders. J Vis Exp :
Gall, Joseph G (2016) DNA replication and beyond. Nat Rev Mol Cell Biol 17:464
Gall, Joseph G (2016) The origin of in situ hybridization - A personal history. Methods 98:4-9
Nizami, Zehra F; Liu, Ji-Long; Gall, Joseph G (2015) Fluorescent In Situ Hybridization of Nuclear Bodies in Drosophila melanogaster Ovaries. Methods Mol Biol 1328:137-49

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