{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,9,22]],"date-time":"2026-09-22T00:58:24Z","timestamp":1790038704633,"version":"4.0.1"},"reference-count":80,"publisher":"American Society for Cell Biology (ASCB)","issue":"19","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["MBoC"],"published-print":{"date-parts":[[2018,9,15]]},"abstract":"<jats:p>Rods and rings (RRs) are large linear- or circular-shaped structures typically described as polymers of IMPDH (inosine monophosphate dehydrogenase). They have been observed across a wide variety of cell types and species and can be induced to form by inhibitors of IMPDH. RRs are thought to play a role in the regulation of de novo guanine nucleotide synthesis; however, the function and regulation of RRs is poorly understood. Here we show that the regulatory GTPase, ARL2, a subset of its binding partners, and several resident proteins at the endoplasmic reticulum (ER) also localize to RRs. We also have identified two new inducers of RR formation: AICAR and glucose deprivation. We demonstrate that RRs can be disassembled if guanine nucleotides can be generated by salvage synthesis regardless of the inducer. Finally, we show that there is an ordered addition of components as RRs mature, with IMPDH first forming aggregates, followed by ARL2, and only later calnexin, a marker of the ER. These findings suggest that RRs are considerably more complex than previously thought and that the function(s) of RRs may include involvement of a regulatory GTPase, its effectors, and potentially contacts with intracellular membranes.<\/jats:p>","DOI":"10.1091\/mbc.e18-05-0274","type":"journal-article","created":{"date-parts":[[2018,7,19]],"date-time":"2018-07-19T15:46:58Z","timestamp":1532015218000},"page":"2303-2316","source":"Crossref","is-referenced-by-count":29,"title":["Compositional complexity of rods and rings"],"prefix":"10.1091","volume":"29","author":[{"given":"Cara R.","family":"Schiavon","sequence":"first","affiliation":[{"name":"Cancer Biology Graduate Program, Graduate Division of Biomedical and Biological Sciences, Laney Graduate School, Atlanta, GA 30307"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Maxwell E.","family":"Griffin","sequence":"additional","affiliation":[{"name":"Cancer Biology Graduate Program, Graduate Division of Biomedical and Biological Sciences, Laney Graduate School, Atlanta, GA 30307"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Marinella","family":"Pirozzi","sequence":"additional","affiliation":[{"name":"EuroBioImaging Facility, Institute of Protein Biochemistry, 80131 Naples, Italy"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Raman","family":"Parashuraman","sequence":"additional","affiliation":[{"name":"EuroBioImaging Facility, Institute of Protein Biochemistry, 80131 Naples, Italy"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Wei","family":"Zhou","sequence":"additional","affiliation":[{"name":"Department of Hematology and Medical Oncology, Emory University School of Medicine, Atlanta, GA 30322"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"H. 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