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Molecular cloning, developmental expression and tissue distribution of diapause hormone and pheromone biosynthesis activating neuropeptide in the bamboo borer O mphisa fuscidentalis
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Abstract
Diapause, an arrested period of post‐embryonic development in insects, is under the control of hormonal interactions. In the bamboo borer
Omphisa fuscidentalis
H
ampson (
L
epidoptera:
C
rambidae), larvae remain in diapause for as long as 9 months during the dry season, from
S
eptember to the following
J
une, although the factors that regulate larval diapause are poorly understood. The present study describes the cloning and expression analysis of the diapause hormone and pheromone biosynthesis activating neuropeptide (
DH‐PBAN
) precursor of
O. fuscidentalis
(
Ompfu‐
DH‐PBAN
cDNA
), aiming to reveal how it may be involved regulating larval diapause in this species in combination with environmental factors. The open reading frame (
ORF
) of the
cDNA
encodes a 199‐amino acid precursor protein that contains
DH
,
PBAN
and three other neuropeptides, all of which share a conservative
C
‐terminal pentapeptide motif
FXPR
/
KL
(
X
=
G
,
T
or
S
). The
Ompfu‐
DH‐PBAN
is highly similar (74%) to the
DH‐PBAN
of the legume pod borer (
Maruca vitrata
). A quantitative real‐time
polymerase chain reaction
reveals that
Ompfu‐
DH‐PBAN
mRNA
is expressed only in neural tissues and that expression is highest in the suboesophageal ganglion. In addition, the expression level of
Ompfu‐
DH‐PBAN
mRNA
in the suboesophageal ganglion is consistently high during the fifth larval instar, increasing moderately in early diapause before reaching a peak during late diapause. After pupation, expression of the
O
mpfu‐
DH‐PBAN
precursor decreases to a low level. In addition to endocrine factors, the results demonstrate that photoperiod increases the expression level of
Ompfu‐
DH‐PBAN
mRNA
in larval diapause. These results also suggest that the expression of the
Ompfu‐
DH‐PBAN
gene correlates with larval diapause development and may be activated by photoperiod in
O. fuscidentalis
.
Title: Molecular cloning, developmental expression and tissue distribution of diapause hormone and pheromone biosynthesis activating neuropeptide in the bamboo borer
O
mphisa fuscidentalis
Description:
Abstract
Diapause, an arrested period of post‐embryonic development in insects, is under the control of hormonal interactions.
In the bamboo borer
Omphisa fuscidentalis
H
ampson (
L
epidoptera:
C
rambidae), larvae remain in diapause for as long as 9 months during the dry season, from
S
eptember to the following
J
une, although the factors that regulate larval diapause are poorly understood.
The present study describes the cloning and expression analysis of the diapause hormone and pheromone biosynthesis activating neuropeptide (
DH‐PBAN
) precursor of
O.
fuscidentalis
(
Ompfu‐
DH‐PBAN
cDNA
), aiming to reveal how it may be involved regulating larval diapause in this species in combination with environmental factors.
The open reading frame (
ORF
) of the
cDNA
encodes a 199‐amino acid precursor protein that contains
DH
,
PBAN
and three other neuropeptides, all of which share a conservative
C
‐terminal pentapeptide motif
FXPR
/
KL
(
X
=
G
,
T
or
S
).
The
Ompfu‐
DH‐PBAN
is highly similar (74%) to the
DH‐PBAN
of the legume pod borer (
Maruca vitrata
).
A quantitative real‐time
polymerase chain reaction
reveals that
Ompfu‐
DH‐PBAN
mRNA
is expressed only in neural tissues and that expression is highest in the suboesophageal ganglion.
In addition, the expression level of
Ompfu‐
DH‐PBAN
mRNA
in the suboesophageal ganglion is consistently high during the fifth larval instar, increasing moderately in early diapause before reaching a peak during late diapause.
After pupation, expression of the
O
mpfu‐
DH‐PBAN
precursor decreases to a low level.
In addition to endocrine factors, the results demonstrate that photoperiod increases the expression level of
Ompfu‐
DH‐PBAN
mRNA
in larval diapause.
These results also suggest that the expression of the
Ompfu‐
DH‐PBAN
gene correlates with larval diapause development and may be activated by photoperiod in
O.
fuscidentalis
.
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