Cloning, characterization, and expression of LeEIL-1, an Arabidopsis EIN3 homolog, in Lithospermum erythrorhizon
Ethylene is a crucial signal in regulating the biosynthesis of shikonin in Lithospermum erythrorhizon . Arabidopsis ethylene-insensitive 3 (EIN3) is the key transcriptional factor of the ethylene signal transduction pathway; thus, EIN3 homologs might play an important role in shikonin formation. Her...
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Veröffentlicht in: | Plant cell, tissue and organ culture tissue and organ culture, 2011-07, Vol.106 (1), p.71-79 |
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Zusammenfassung: | Ethylene is a crucial signal in regulating the biosynthesis of shikonin in
Lithospermum erythrorhizon
.
Arabidopsis
ethylene-insensitive 3 (EIN3) is the key transcriptional factor of the ethylene signal transduction pathway; thus, EIN3 homologs might play an important role in shikonin formation. Here,
LeEIL
-
1
, a gene with high similarity to EIN3, was cloned from
L. erythrorhizon
using a combination method of touch-down PCR and rapid amplification of cDNA ends. The full-length cDNA of
LeEIL
-
1
is 2,359 bp, encoding a polypeptide of 635 amino acids. By inserting the entire coding region of
LeEIL
-
1
into the pET32a (+) expression vector, the prokaryotic expression of
LeEIL
-
1
was successfully induced by isopropyl β-
d
-1-thiogalactopyranoside in BL21(DE3)pLysS cells. Moreover, the recombinant LeEIL-1 protein was verified by western blotting with the
Arabidopsis
anti-EIN3 antibody
.
Real-time PCR results show that the mRNA level of
LeEIL
-
1
was first dramatically induced within 3 h when the
L. erythrorhizon
cells were transferred from B5 to M9 medium for shikonin formation; subsequently, the transcripts of
LeEIL
-
1
decreased to a relatively stable level. Tissue-specific expression analysis indicates that less
LeEIL
-
1
mRNA accumulated in the stem and leaf than in the root, where shikonin was biosynthesized. These results imply that
LeEIL
-
1
could be a possible reverse genetic target for revealing the relationship between ethylene and shikonin formation. |
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ISSN: | 0167-6857 1573-5044 |
DOI: | 10.1007/s11240-010-9895-1 |