Excised lettuce (Lactuca sativa L.) hypocotyl sections retain the ability to elongate in response to gibberellic acid (GA3) addition. In 48 hr at 30 C a GA3-treated segment more than doubles while a control segment elongates less than 50%70. Auxin has no detectable effect on this system. Sensitivity to GA3 is not decreased by apex or root removal. Of the experimental variables tested, temperature, sucrose, and preincubation in water affect growth both with and without GA3. Blue and far red light inhibit growth without GAs; this inhibition is reversed by GA3. Potassium chloride stimulates growth of illuminated sections treated with GA3 but has no effect on control growth. When sections are incubated in the dark, KCl has a promotive effect on elongation.There are numerous advantages to using excised plant segments to study the mechanism of hormone action. Interactions, such as transport of hormones and nutrients to the responding segment, are eliminated as variables. The recent advances which have been made in the characterization of the auxin response clearly demonstrate the utility of such isolated segments (4, 5).Research on the mechanism of gibberellin-induced elongation has been hampered by an apparent diminution in ability to respond to GA3 when stem segments are removed from meristematic regions (10). Recently, Kaufman and his colleagues (9,13,14,19) demonstrated a dramatic effect of GA3 on growth of excised stem segments of Avena, but sections from dicotyledonous plants have seemed less responsive. Brian and Hemming (1) showed that the growth of segments from dwarf pea stems was much less than that realized by similar regions of whole plants and was not elevated by GA3 application. Furthermore, the GA3 response of many isolated sections has been shown to be dependent on added auxin (1,27,30) or sucrose (24). This paper describes the GA3-induced growth of sections isolated from the hypocotyl of lettuce seedlings.
MATERILS AND METHODSPlant Material. Seeds of lettuce (Lactuca sativa L. cv. Arctic) were obtained from Carter's Ltd., Raynes Park, London. Seeds were imbibed for 2 hr in an excess of distilled H20 and were sown in white light in 9-cm Petri dishes on a circle of Whatman No. 1 filter paper wetted with 5 ml of distilled H20. Germination proceeded in the dark at 25 C for 34 hr after which time the