|
Plant Physiol, January 2003, Vol. 131, pp. 276-286
Ethylene Biosynthesis in Detached Young Persimmon Fruit Is
Initiated in Calyx and Modulated by Water Loss from the
Fruit1
Ryohei
Nakano,*
Emi
Ogura,
Yasutaka
Kubo, and
Akitsugu
Inaba
Laboratory of Postharvest Agriculture, Faculty of Agriculture,
Okayama University, Tsushima, Okayama 700-8530, Japan
Persimmon (Diospyros kaki Thunb.) fruit are
usually classified as climacteric fruit; however, unlike typical
climacteric fruits, persimmon fruit exhibit a unique characteristic in
that the younger the stage of fruit detached, the greater the level of
ethylene produced. To investigate ethylene induction mechanisms in
detached young persimmon fruit, we cloned three cDNAs encoding
1-aminocyclopropane-1-carboxylic acid (ACC) synthase
(DK-ACS1, 2, and
-3) and two encoding ACC oxidase
(DK-ACO1 and -2) genes
involved in ethylene biosynthesis, and we analyzed their expression in
various fruit tissues. Ethylene production was induced within a few
days of detachment in all fruit tissues tested, accompanied by
temporally and spatially coordinated expression of all the
DK-ACS and
DK-ACO genes. In all tissues except the
calyx, treatment with 1-methylcyclopropene, an inhibitor of ethylene
action, suppressed ethylene production and ethylene
biosynthesis-related gene expression. In the calyx, one ACC synthase
gene (DK-ACS2) exhibited increased mRNA
accumulation accompanied by a large quantity of ethylene production,
and treatment of the fruit with 1-methylcyclopropene did not prevent
either the accumulation of DK-ACS2
transcripts or ethylene induction. Furthermore, the alleviation of
water loss from the fruit significantly delayed the onset of ethylene
production and the expression of DK-ACS2
in the calyx. These results indicate that ethylene biosynthesis in
detached young persimmon fruit is initially induced in calyx and is
modulated by water loss through transcriptional activation of
DK-ACS2. The ethylene produced in the
calyx subsequently diffuses to other fruit tissues and acts as a
secondary signal that stimulates autocatalytic ethylene biosynthesis in
these tissues, leading to a burst of ethylene production.
1
This work was supported in part by the Ministry
of Education, Science, Sports and Culture of Japan (Grant-in-Aid for
Young Scientists no. 13760023 to R.N. and Grant-in-Aid for Scientific Research no. 14560023 to Y.K.) and by the Ministry of Agriculture, Forestry and Fisheries of Japan (research project for utilizing advanced technologies in agriculture, forestry and fisheries no. 1421 to R.N.).
*
Corresponding author; e-mail rnakano{at}cc.okayama-u.ac.jp; fax
81-86-251-8338.
© 2003 American Society of Plant Biologists
This article has been cited by other articles:

|
 |

|
 |
 
J. Xue, Y. Li, H. Tan, F. Yang, N. Ma, and J. Gao
Expression of ethylene biosynthetic and receptor genes in rose floral tissues during ethylene-enhanced flower opening
J. Exp. Bot.,
May 1, 2008;
59(8):
2161 - 2169.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
A. Inaba, X. Liu, N. Yokotani, M. Yamane, W.-J. Lu, R. Nakano, and Y. Kubo
Differential feedback regulation of ethylene biosynthesis in pulp and peel tissues of banana fruit
J. Exp. Bot.,
March 1, 2007;
58(5):
1047 - 1057.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
N. Ma, H. Tan, X. Liu, J. Xue, Y. Li, and J. Gao
Transcriptional regulation of ethylene receptor and CTR genes involved in ethylene-induced flower opening in cut rose (Rosa hybrida) cv. Samantha
J. Exp. Bot.,
August 1, 2006;
57(11):
2763 - 2773.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
R. Yuan, Z. Wu, I. A. Kostenyuk, and J. K. Burns
G-protein-coupled {alpha}2A-adrenoreceptor agonists differentially alter citrus leaf and fruit abscission by affecting expression of ACC synthase and ACC oxidase
J. Exp. Bot.,
July 1, 2005;
56(417):
1867 - 1875.
[Abstract]
[Full Text]
[PDF]
|
 |
|
|
|