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Alterations in ribosome biogenesis cause ... ans hermaphrodite gonadogenesis


Alterations in ribosome biogenesis cause specific defects in C elegans hermaphrodite gonadogenesis

5384

Ribosome biogenesis is a cell-essential process that influences cell growth, proliferation, and differentiation. How ribosome biogenesis impacts development, however, is poorly understood. Here, we establish a link between ribosome biogenesis and gonadogenesis in Caenorhabditis elegans that affects germline proliferation and patterning. Previously, we determined that pro-1(+)activity is required in the soma--specifically, the sheath/spermatheca sublineage--to promote normal proliferation and prevent germline tumor formation. Here, we report that PRO-1, like its yeast ortholog IPI3, influences rRNA processing. pro-1 tumors are suppressed by mutations in ncl-1 or lin-35/Rb, both of which elevate pre-rRNA levels. Thus, in this context, lin-35/Rb acts as a soma-autonomous germline tumor promoter. We further report the characterization of two additional genes identified for their germline tumor phenotype, pro-2 and pro-3, and find that they, too, encode orthologs of proteins involved in ribosome biogenesis in yeast (NOC2 and SDA1, respectively). Finally, we demonstrate that depletion of additional C. elegans orthologs of yeast ribosome biogenesis factors display phenotypes similar to depletion of progenes. We conclude that the C. elegans distal sheath is particularly sensitive to alterations in ribosome biogenesis and that ribosome biogenesis defects in one tissue can non-autonomously influence proliferation in an adjacent tissue.


Voutev R, Killian DJ, Ahn JH, Hubbard EJ

Developmental biology

2006-10-01 00:00

298

1

45-58

Amino Acid Sequence,Animals,Body Patterning,Caenorhabditis elegans,Caenorhabditis elegans Proteins,Cell Nucleolus,Germ Cells,Gonads,Hermaphroditism,Molecular Sequence Data,Phenotype,RNA Interference,RNA, Ribosomal,Repressor Proteins,Ribosomes,Sequence Homology, Amino Acid,Caenorhabditis elegans Proteins,RNA, Ribosomal,Repressor Proteins,lin-35 protein, C elegans

Department of Biology, New York University, New York, NY 10003-6688, USA.

Dev. Biol.

NIGMS GM61706

0012-1606

10.1016/j.ydbio.2006.06.011

S0012-1606(06)00912-2

0

False

16876152

Darrell Killian
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