Three Tnt1 subfamilies show different stress-associated patterns of expression in tobacco. Consequences for retrotransposon control and evolution in plants

Citation
T. Beguiristain et al., Three Tnt1 subfamilies show different stress-associated patterns of expression in tobacco. Consequences for retrotransposon control and evolution in plants, PLANT PHYSL, 127(1), 2001, pp. 212-221
Citations number
42
Categorie Soggetti
Plant Sciences","Animal & Plant Sciences
Journal title
PLANT PHYSIOLOGY
ISSN journal
00320889 → ACNP
Volume
127
Issue
1
Year of publication
2001
Pages
212 - 221
Database
ISI
SICI code
0032-0889(200109)127:1<212:TTSSDS>2.0.ZU;2-4
Abstract
The genomes of most Nicotiana species contain three different subfamilies o f the Tnt1 retrotransposon, which differ completely in their U3 sequence, w hereas the rest of the sequence is relatively constant. The results present ed here show that all three Tnt1 subfamilies are expressed in tobacco (Nico tiana tabacum) and that the U3 sequence variability correlates with differe nces in the pattern of expression of the Tnt1 elements. Each of the three T nt1 subfamilies is induced by stress, but their promoters have a different response to different stress-associated signaling molecules. The Tnt1A subf amily is particularly strongly induced by elicitors and methyl jasmonate, w hereas expression on the Tn1C subfamily is more sensitive to salicylic acid and auxins. The direct relationship between U3 sequence variability and di fferences in the stress-associated expression of the Tnt1 elements present in a single host species gives support to our model that postulates that re trotransposons have adapted to their host genomes through the evolution of highly regulated promoters that mimic those of the stress-induced plant gen es. Moreover, here we show that the analysis of the transcriptional control of a retrotransposon population such as Tnt1 provides new insights into th e study of the complex and still poorly understood network of defense- and stress-induced plant signal transduction pathways.