1. Academic Validation
  2. Biochemical basis for the biological clock

Biochemical basis for the biological clock

  • Biochemistry. 2002 Oct 8;41(40):11941-5. doi: 10.1021/bi020392h.
D James Morré 1 Pin-Ju Chueh Jake Pletcher Xiaoyu Tang Lian-Ying Wu Dorothy M Morré
Affiliations

Affiliations

  • 1 Department of Medicinal Chemistry and Molecular Pharmacology, 136 Hansen Life Sciences Research Building, Purdue University, West Lafayette, IN 47907, USA. morre@pharmacy.purdue.edu
  • 2 Purdue U, West Lafayette, IN
Abstract

NADH oxidases at the external surface of plant and animal cells (ECTO-NOX proteins) exhibit stable and recurring patterns of oscillations with potentially clock-related, entrainable, and temperature-compensated period lengths of 24 min. To determine if ECTO-NOX proteins might represent the ultradian time keepers (pacemakers) of the biological clock, COS cells were transfected with cDNAs encoding tNOX proteins having a period length of 22 min or with C575A or C558A cysteine to alanine replacements having period lengths of 36 or 42 min. Here we demonstrate that such transfectants exhibited 22, 36, or 40 to 42 h circadian patterns in the activity of glyceraldehyde-3-phosphate dehydrogenase, a common clock-regulated protein, in addition to the endogenous 24 h circadian period length. The fact that the expression of a single oscillatory ECTO-NOX protein determines the period length of a circadian biochemical marker (60 X the ECTO-NOX period length) provides compelling evidence that ECTO-NOX proteins are the biochemical ultradian drivers of the cellular biological clock.

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