Regulation of Ribosome Biogenesis by Nucleostemin 3 Promotes Local and Systemic Growth in Drosophila

Author:

Hartl Tom A1,Ni Julie1,Cao Jian1,Suyama Kaye L1,Patchett Stephanie2,Bussiere Cyril3,Gui Dan Yi1,Tang Sheng1,Kaplan Daniel D1,Fish Matthew1,Johnson Arlen W2,Scott Matthew P1

Affiliation:

1. Departments of Developmental Biology, Genetics, and Bioengineering, Howard Hughes Medical Institute, Stanford University School of Medicine, Stanford, California 94305

2. Section of Molecular Genetics and Microbiology and the Institute for Cell and Molecular Biology, University of Texas, Austin, Texas 78712

3. School of Medicine, Texas Tech University Health Sciences Center, Lubbock, Texas 79415

Abstract

Abstract Nucleostemin 3 (NS3) is an evolutionarily conserved protein with profound roles in cell growth and viability. Here we analyze cell-autonomous and non-cell-autonomous growth control roles of NS3 in Drosophila and demonstrate its GTPase activity using genetic and biochemical assays. Two null alleles of ns3, and RNAi, demonstrate the necessity of NS3 for cell autonomous growth. A hypomorphic allele highlights the hypersensitivity of neurons to lowered NS3 function. We propose that NS3 is the functional ortholog of yeast and human Lsg1, which promotes release of the nuclear export adapter from the large ribosomal subunit. Release of the adapter and its recycling to the nucleus are essential for sustained production of ribosomes. The ribosome biogenesis role of NS3 is essential for proper rates of translation in all tissues and is necessary for functions of growth-promoting neurons.

Publisher

Oxford University Press (OUP)

Subject

Genetics

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