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DNA barcoding of Actinidia (Actinidiaceae) using internal transcribed spacer, matK , rbcL and trnH
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ABSTRACT
Actinidia
is taxonomically difficult and economically important. Four traditional barcoding markers, internal transcribed spacer (ITS),
rbcL
,
matK
and
trnH
‐
psbA
, were used to identify the 29
Actinidia
species sampled. High‐quality sequences could be obtained easily for
rbcL
,
matK
and
trnH
‐
psbA
, and
matK
performed best at resolving species among these three markers. ITS had a moderate sequencing success of 72% and the species resolution proportion was 60.7%. Sequencing success rate for
matK
+
rbcL
was 97.4% and it discriminated 48.3% of the species analysed. The barcode
trnH
‐
psbA
could only identify
Actinidia eriantha. MatK
+
rbcL
and ITS are useful markers to barcode
Actinidia
; the utility of ITS in barcoding needs further investigation using high‐throughput sequencing technology. Phylogenetic analyses based on ITS,
matK
,
matK
+
rbcL
and
matK
+
rbcL
+
trnH
‐
psbA
indicated Sect.
Leiocarpae
to be paraphyletic, while Sect.
Maculatae
and Sect.
Strigosae
together with Sect.
Stellatae
formed a monophyletic group. We recommended the subdivision of
Actinidia
into two groups: one consisting of Sect.
Leiocarpae
(ovaries glabrous, fruits spotless), and the other comprising sections
Maculatae
,
Strigosae
and
Stellatae
(ovaries hairy, fruits spotted). This study supported the separation of
Actinidia chinensis
var.
chinensis
and var.
deliciosa
at the infraspecific level, and the separation of
Actinidia tetramera
and
Actinidia kolomikta
at the specific level. The treatment of
Actinidia maloides
as a synonym of
A
.
kolomikta
and
Actinidia cinerascen
s as a variety of
Actinidia fulvicoma
was also warranted.
Title: DNA barcoding of
Actinidia
(Actinidiaceae) using internal transcribed spacer,
matK
,
rbcL
and
trnH
Description:
ABSTRACT
Actinidia
is taxonomically difficult and economically important.
Four traditional barcoding markers, internal transcribed spacer (ITS),
rbcL
,
matK
and
trnH
‐
psbA
, were used to identify the 29
Actinidia
species sampled.
High‐quality sequences could be obtained easily for
rbcL
,
matK
and
trnH
‐
psbA
, and
matK
performed best at resolving species among these three markers.
ITS had a moderate sequencing success of 72% and the species resolution proportion was 60.
7%.
Sequencing success rate for
matK
+
rbcL
was 97.
4% and it discriminated 48.
3% of the species analysed.
The barcode
trnH
‐
psbA
could only identify
Actinidia eriantha.
MatK
+
rbcL
and ITS are useful markers to barcode
Actinidia
; the utility of ITS in barcoding needs further investigation using high‐throughput sequencing technology.
Phylogenetic analyses based on ITS,
matK
,
matK
+
rbcL
and
matK
+
rbcL
+
trnH
‐
psbA
indicated Sect.
Leiocarpae
to be paraphyletic, while Sect.
Maculatae
and Sect.
Strigosae
together with Sect.
Stellatae
formed a monophyletic group.
We recommended the subdivision of
Actinidia
into two groups: one consisting of Sect.
Leiocarpae
(ovaries glabrous, fruits spotless), and the other comprising sections
Maculatae
,
Strigosae
and
Stellatae
(ovaries hairy, fruits spotted).
This study supported the separation of
Actinidia chinensis
var.
chinensis
and var.
deliciosa
at the infraspecific level, and the separation of
Actinidia tetramera
and
Actinidia kolomikta
at the specific level.
The treatment of
Actinidia maloides
as a synonym of
A
.
kolomikta
and
Actinidia cinerascen
s as a variety of
Actinidia fulvicoma
was also warranted.
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