EXPRESSION OF A LUTEOVIRAL MOVEMENT PROTEIN IN TRANSGENIC PLANTS LEADS TO CARBOHYDRATE ACCUMULATION AND REDUCED PHOTOSYNTHETIC CAPACITY IN-SOURCE LEAVES
K. Herbers et al., EXPRESSION OF A LUTEOVIRAL MOVEMENT PROTEIN IN TRANSGENIC PLANTS LEADS TO CARBOHYDRATE ACCUMULATION AND REDUCED PHOTOSYNTHETIC CAPACITY IN-SOURCE LEAVES, Plant journal, 12(5), 1997, pp. 1045-1056
Elucidating the role of viral genes in transgenic plants revealed that
the movement protein (MP) from tobacco mosaic virus is responsible fo
r altered carbohydrate allocation in tobacco and potato plants. To stu
dy whether this is a general feature of viral MPs, the movement protei
n MP17 of potato leafroll virus (PLRV), a phloem-restricted luteovirus
, was constitutively expressed in tobacco plants. Transgenic lines wer
e strongly reduced in height and developed bleached and sometimes even
necrotic areas on their source leaves. Levels of soluble sugars and s
tarch were significantly increased in source leaves. Yet, in leaf lami
nae the hexose-phosphate content was unaltered and ATP reduced to only
a small extent, indicating that these leaves were able to maintain ho
meostatic conditions by compartmentalization of soluble sugars, probab
ly in the vacuole. On the contrary, midribs contained lower levels of
soluble sugars, ATP, hexose-phosphates and UDP-glucose supporting the
concept of limited uptake and catabolism of sucrose in the phloem. The
accumulation of carbohydrates led to a decreased photosynthetic capac
ity and carboxylation efficiency of ribulose-1,5-bisphosphate carboxyl
ase/oxygenase (rubisco) probably owing to decreased expression of phot
osynthetic proteins. In parallel, levels of pathogenesis-related prote
ins were elevated which may be the reason for the obtained limited res
istance against the unrelated potato virus Y (PVY)(N) in the transgeni
c tobacco plants. Ultrathin sections of affected leaves harvested from
2-week-old plants revealed plasmodesmal alterations in the phloem tis
sue while plasmodesmata between mesophyll cells were indistinguishable
from wild-type. These data favour the phloem tissue to be the primary
site of PLRV MP17 action in altering carbohydrate metabolism.