Abstrakt interacts with and regulates the expression of sorting nexin-2

• Published in: Journal of cellular physiology Vol. 204; no. 1; pp. 210 - 218
• Main Authors: Abdul-Ghani, Mohammad, Hartman, Kristin L., Ngsee, Johnny K.
• Format: Journal Article
• Language: English
• Published: Hoboken Wiley Subscription Services, Inc., A Wiley Company 01.07.2005
• Subjects: Animals; Carrier Proteins - chemistry; Carrier Proteins - genetics; Carrier Proteins - metabolism; Cell Nucleus - metabolism; CHO Cells; Cricetinae; Culture Media, Serum-Free - pharmacology; Cytoplasm - metabolism; DEAD-box RNA Helicases; Gene Expression; Humans; Protein Structure, Tertiary; Protein Transport - physiology; RNA Helicases - chemistry; RNA Helicases - genetics; RNA Helicases - metabolism; RNA, Messenger - metabolism; Vesicular Transport Proteins - chemistry; Vesicular Transport Proteins - genetics; Vesicular Transport Proteins - metabolism
• ISSN: 0021-9541; 1097-4652
• DOI: 10.1002/jcp.20285

Protein sorting through vesicular compartments is highly regulated to maintain the integrity and signaling of intracellular organelles in eukaryotic cells. Sorting Nexin‐2 (SNX2) is involved in protein sorting in the trans‐Golgi network, endosome, and/or lysosome compartments, with loss of function leading to defect in protein sorting and stress on organelles. To investigate the function of SNX2, we have identified the DEAD‐box helicase Abstrakt (Abs) as an SNX2‐interacting protein. The N‐terminal domain of Abs interacts with the phox homology (PX) domain of SNX2 suggesting that PX domains may also participate in protein–protein interaction. Interestingly, both proteins undergo nucleocytoplasmic shuttling, and this process is responsive to serum withdrawal for Abs. Finally, expression of Abs reduced the cellular expression of SNX2 without altering its steady state mRNA levels. This unexpected interaction provides a novel mechanism whereby expression of proteins involved in membrane trafficking could be regulated by an RNA helicase. © 2005 Wiley‐Liss, Inc.