IRON-DEPENDENT PROTECTION OF THE SYNECHOCOCCUS FERREDOXIN-I TRANSCRIPT AGAINST NUCLEOLYTIC DEGRADATION REQUIRES CIS-REGULATORY SEQUENCES INTHE 5' PART OF THE MESSENGER-RNA
A. Bovy et al., IRON-DEPENDENT PROTECTION OF THE SYNECHOCOCCUS FERREDOXIN-I TRANSCRIPT AGAINST NUCLEOLYTIC DEGRADATION REQUIRES CIS-REGULATORY SEQUENCES INTHE 5' PART OF THE MESSENGER-RNA, Plant molecular biology, 22(6), 1993, pp. 1047-1065
We have previously reported that the ferredoxin I gene from Synechococ
cus sp. PCC 7942 is regulated by iron at the level of differential mRN
A stability. To identify iron-responsive elements in the Synechococcus
ferredoxin transcript, we have tested chimaeric constructs containing
translational fusions between the Synechococcus and the Anabaena sp.
PCC 7937 ferredoxin genes for iron-dependent expression in transgenic
Synechococcus strains. This strategy was based on the observation that
the level of the Anabaena ferredoxin MRNA did not increase upon iron
addition in Synechococcus. Our results show that the presence of the f
irst 207 nucleotides of the Synechococcus ferredoxin transcript is suf
ficient to confer iron responsiveness to the chimaeric transcripts. Th
is iron responsiveness was accomplished by an increased stability of t
he chimaeric transcript in the presence of iron, as was found for the
intact Synechococcus ferredoxin gene. Addition of the translation inhi
bitor chloramphenicol to the cultures led to a rapid stabilization, in
low- and high-iron conditions, of the wild-type Synechococcus ferredo
xin transcript as well as all chimaeric ferredoxin transcripts tested.
These results suggest the existence of a constitutively expressed nuc
lease capable of degrading the ferredoxin transcripts. They further su
pport the suggestion that the first 207 nucleotides of the Synechococc
us transcript contain a specific sequence that is recognized by an iro
n-responsive factor and that this interaction leads to protection agai
nst degradation.