The regulation of cambial activity in C hinese fir ( C unninghamia lanceolata ) involves extensive transcriptome remodeling
Summary C hinese fir ( C unninghamia lanceolata ), a commercially important tree for the timber and pulp industry, is widely distributed in southern C hina and northern V ietnam, but its large and complex genome has hindered the development of genomic resources. Few efforts have focused on analysis...
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Published in | The New phytologist Vol. 199; no. 3; pp. 708 - 719 |
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Main Authors | , , , , , , , |
Format | Journal Article |
Language | English |
Published |
01.08.2013
|
Online Access | Get full text |
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Summary: | Summary
C
hinese fir (
C
unninghamia lanceolata
), a commercially important tree for the timber and pulp industry, is widely distributed in southern
C
hina and northern
V
ietnam, but its large and complex genome has hindered the development of genomic resources. Few efforts have focused on analysis of the modulation of transcriptional networks in vascular cambium during the transition from active growth to dormancy in conifers.
Here, we used
I
llumina sequencing to analyze the global transcriptome alterations at the different stages of vascular cambium development in
C
hinese fir.
By analyzing dynamic changes in the transcriptome of vascular cambium based on our RNA sequencing (
RNA
‐
S
eq) data at the dormant, reactivating and active stages, many potentially interesting genes were identified that encoded putative regulators of cambial activity, cell division, cell expansion and cell wall biosynthesis and modification. In particular, the genes involved in transcriptional regulation and hormone signaling were highlighted to reveal their biological importance in the cambium development and wood formation.
Our results reveal the dynamics of transcriptional networks and identify potential key components in the regulation of vascular cambium development in
C
hinese fir, which will contribute to the in‐depth study of cambial differentiation and wood‐forming candidate genes in conifers. |
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ISSN: | 0028-646X 1469-8137 |
DOI: | 10.1111/nph.12301 |