Identification and characterization of GRIM-1, a cell-death-associated gene product

Author:

Hofmann Edward R.1,Nallar Shreeram C.1,Lin Limei1,D'Cunha Jonathan1,Lindner Daniel J.2,Weihua Xiao3,Kalvakolanu Dhananjaya V.1

Affiliation:

1. Greenebaum Cancer Center, Department of Microbiology and Immunology, Molecular and Cellular Cancer Biology Track, GPILS, University of Maryland School of Medicine, Baltimore, MD 21201, USA

2. Taussig Cancer Center, Lerner Research Institute, Cleveland, OH 44195, USA

3. Hefei National Laboratory of Physical Sciences at Microscale, University of Science and Technology, Hefei, Anhui 230027, China

Abstract

Using a genome-wide technical knockout, we isolated a newly identified set of GRIM (genes associated with retinoid-interferon-induced mortality) genes; GRIM genes mediate IFN- and retinoic-acid (RA)-induced cell death. Here, we describe the isolation and characterization of one such gene, GRIM-1. Three proteins, with identical C-termini, were produced from the GRIM-1 open reading frame when this gene was transcribed and translated in vitro. These protein isoforms, designated GRIM-1α, GRIM-1β and GRIM-1γ, differentially suppressed growth via apoptosis in various cell lines. We also show that a caspase-dependent mechanism generates the proapoptotic GRIM-1 isoforms. Lastly, GRIM-1 isoforms differentially blocked maturation of 18S ribosomal RNA, consistent with their respective growth-suppressive ability. Together, these studies identified a novel protein involved in growth suppression and cell death.

Publisher

The Company of Biologists

Subject

Cell Biology

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