No.42 - è¾²æ¥çç©è³æºç 究æ
No.42 - è¾²æ¥çç©è³æºç 究æ
No.42 - è¾²æ¥çç©è³æºç 究æ
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MECHANISM OF BRASSINOSTEROID SIGNALING<br />
55<br />
plants under dark conditions causes phenotypes similar to those displayed by brassinosteroiddeficient<br />
mutants, such as shortened hypocotyl, cotyledon opening, and de-etiolation. In the light,<br />
plants treated with the Brz displayed dwarf and highly greened leaves (Asami et al., 2000, Asami<br />
and Yoshida, 1999). In the stem tissues, development of the vascular bundle cells was inhibited by<br />
Brz. (Nagata et al., 2001)<br />
The Brz also revealed the regulation of chloroplast development by brassinosteroid. In the<br />
cotyledon of dark-germinated plant, the mRNA of chloroplast genes; i.e., cab and rbcS, did not<br />
expressed. But, in the cotyledon of dark-germinated plant with Brz, these chloroplast genes<br />
expression was detected (Asami et al., 2000, Nagata et al., 2000). After 2 hour light emission to<br />
these dark-germinated plant, the Brz-treated plant harbored very quick developed chloroplast that<br />
contained more numbered thylakoid membrane layer that Brz-untreated plant. These result<br />
revealed that plastid development was regulated brassinosteroid. (Fig. 2)<br />
Brassinosteroid receper BRI1<br />
The Arabidopsis bri1 mutant was also identified by its dwarf phenotype, but brassinosteroid<br />
treatment did not recover the dwarfism to wild-type phenotype and did not inhibit the elongation of<br />
the roots of this mutant (Clouse et al., 1996, Li and Chory, 1997) (Fig. 3). Study of bri1 revealed<br />
that BRI1 is a critical component in brassinosteroid signaling, and that mutation in its BRI1 gene<br />
Fig. 2 Brz effect to the plant.<br />
Brz treatment of plants under dark conditions causes photomorphogenesis such as shortened<br />
hypocotyl, cotyledon opening. In the light, plants treated with the Brz displayed dwarf and highly<br />
greened leaves. The Brz also revealed the regulation of chloroplast development by brassinosteroid.