Dark-grown cells of Euglena contain proplastids which, upon exposure to light, differentiate into chloroplasts. During this process, structural and functional changes occur, including the synthesis of pigments, enzymes of photosynthetic electron transport, enzymes of CO2 reduction, chloroplast membrane proteins, and lipids and chloroplast ribosomes (36).Holowinsky and Schiff (17) In addition to the increase of plastid DNA during chloroplast development, Manning and Richards (24) noted that chloroplast DNA undergoes one and one-half rounds of DNA replication per one round of nuclear DNA replication, yet the amount of chloroplast DNA per cell remains constant. They postulated that a mechanism must exist to remove the "extra" DNA. Egan, Dorsky and Schiff (12) reported the light activation of a chloroplast associated DNase. This enzyme was further characterized by Small and Sturgen (40). The action spectrum for the light activation of the nuclease is similar to the action spectrum for the synthesis of Chl and some chloroplast-associated enzymes. Schmidt and Lyman (unpublished data) found that the amount of chloroplast DNA per cell increases in high intensities of blue light. All this evidence suggests the operation of a mechanism to regulate the amount of plastid DNA during chloroplast development as well as during growth. Regulation seems to be operating to keep the amount of chloroplast DNA constant because there is more DNA synthesized per chloroplast division than is needed for merely doubling the DNA content (24).In this paper, we propose that such regulation may occur through a restriction-type nuclease which degrades a fraction of the chloroplast DNA. We also propose that the putative nuclease is activated by the red-blue photomorphogenic system which mediates, with the blue chromophore, chloroplast development.Chloroplast DNA in Euglena constitutes 3 to 5% of the total cellular DNA (39