Identification and expression of three new Nicotiana plumbaginifolia genes which encode isoforms of a plasma-membrane H+-ATPase, and one of which is induced by mechanical stress

被引:72
作者
Oufattole, M [1 ]
Arango, M [1 ]
Boutry, M [1 ]
机构
[1] Catholic Univ Louvain, Unite Biochim Physiol, B-1348 Louvain, Belgium
关键词
gene family; H+-ATPase; Nicotiana; plasma membrane;
D O I
10.1007/s004250050672
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
To analyze in detail the multigene family encoding the plasma-membrane H+-ATPase (pma) in Nicotiana plumbaginifolia Viv., five new pma genes (pma 5-9) were isolated. Three of these (pma 6, 8, 9) were fully characterized and classified into new and independent subfamilies. Their cell-type expression was followed by the beta-glucuronidase (gusA) reporter-gene method. While the pma8-gusA transgene was not expressed in transgenic tobacco, expression of the two other transgenes (pma6- and pma9-gusA) was found to be restricted to particular cell types. In the vegetative tissues, pma6-gusA expression was limited to the head cells of the leaf short trichomes, involved in secretion, and to the cortical parenchyma of the young nodes where the developing leaves and axillary flowering stalks join the stem. In the latter tissues, gene expression was enhanced by mechanical stress, suggesting that H+-ATPase might be involved in the strength of the tissues and their resistance to mechanical trauma. The pma9-gusA transgene was mainly expressed ill the epical meristem of adventitious roots and axillary buds as well as in the phloem tissues of the stem, in which expression depended on the developmental stage. In flowers, pma9-gusA expression was limited to the mature pollen grains and the young fertilized ovules, while that of pma6-gusA was identified in most of the organs. Reverse transcription-polymerase chain reaction of leaf and stem RNA confirmed the expression of pma 6 and 9, while pma8 was found to be expressed in both organs at a lower level. In conclusion, although pma 6 and 9 had a more restricted expression pattern than the previously characterized pma genes, they were nevertheless expressed in cell types in which H+-ATPase had not been previously detected.
引用
收藏
页码:715 / 722
页数:8
相关论文
共 36 条
[1]  
BEVERLEY SM, 1992, CURRENT PROTOCOLS MO
[2]   MOLECULAR-CLONING OF A FAMILY OF PLANT GENES ENCODING A PROTEIN HOMOLOGOUS TO PLASMA-MEMBRANE H+-TRANSLOCATING ATPASES [J].
BOUTRY, M ;
MICHELET, B ;
GOFFEAU, A .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1989, 162 (02) :567-574
[3]  
BRADFORD MM, 1976, ANAL BIOCHEM, V72, P248, DOI 10.1016/0003-2697(76)90527-3
[4]   Plant cell wall proteins [J].
Cassab, GI .
ANNUAL REVIEW OF PLANT PHYSIOLOGY AND PLANT MOLECULAR BIOLOGY, 1998, 49 :281-309
[5]   Relaxation in a high-stress environment: The molecular bases of extensible cell walls and cell enlargement [J].
Cosgrove, DJ .
PLANT CELL, 1997, 9 (07) :1031-1041
[6]   INSITU ENZYME-HISTOCHEMISTRY ON PLASTIC-EMBEDDED PLANT-MATERIAL - THE DEVELOPMENT OF AN ARTIFACT-FREE BETA-GLUCURONIDASE ASSAY [J].
DEBLOCK, M ;
DEBROUWER, D .
PLANT JOURNAL, 1992, 2 (02) :261-266
[7]   BROAD HOST RANGE DNA CLONING SYSTEM FOR GRAM-NEGATIVE BACTERIA - CONSTRUCTION OF A GENE BANK OF RHIZOBIUM-MELILOTI [J].
DITTA, G ;
STANFIELD, S ;
CORBIN, D ;
HELINSKI, DR .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1980, 77 (12) :7347-7351
[8]  
ENZELL CR, 1980, RECENT ADV TOBACCO S, V6, P64
[9]   ASSESSMENT OF THE NUMBER AND EXPRESSION OF P-TYPE H+-ATPASE GENES IN TOMATO [J].
EWING, NN ;
BENNETT, AB .
PLANT PHYSIOLOGY, 1994, 106 (02) :547-557
[10]   HIGH-LEVEL TUBER EXPRESSION AND SUCROSE INDUCIBILITY OF A POTATO SUS4 SUCROSE SYNTHASE GENE REQUIRE 5'-FLANKING AND 3'-FLANKING SEQUENCES AND THE LEADER INTRON [J].
FU, HY ;
KIM, SY ;
PARK, WD .
PLANT CELL, 1995, 7 (09) :1387-1394