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metabolism but also in photosynthesis, a phylogenetic footprinting is conducted to identify
conserved motifs in intergenic regions of orthologous genes from closely related genomes. Such
a study conducted by Su et al . (2005) on nine cyanobacterial genomes ( G . violaceus PCC 7421,
Anabaena sp. strain PCC 7120, P . marinus strains CCMP1375, MED4 and MIT9313, S . elongatus PCC
6301, Synechococcus sp. strain WH8102, Synechocystis sp. strain PCC 6803 and T . elongatus BP-1)
revealed the existence of strong NtcA promoter regions (i) for the ammonium transporters of the
amt family in all the nine cyanobacterial genomes, and (ii) in the regulatory regions of nirA in all
genomes excepting in Synechococcus sp. strain CCMP1375 and P . marinus MED4. The clustering of
genes of nitrate/nitrite transporters of the ABC-type transporters nrtABCD in Anabaena sp. strain
PCC 7120, G . violaceus PCC 7421, Synechocystis sp. strain PCC 6803, S . elongatus PCC 6301 and
T . elongatus BP-1 with nitrate reductase ( narB ) and nitrite reductase A ( nirA ) and regulator ntcB
upstream of transporters signifi es the regulatory control of all these genes by NtcA. A number of
transcription factors belonging to the families LuxR, LysR, AraC and TetR are encoded by the genome
of A . marina MBIC11017 (Swingley et al ., 2008).
LexA is a transcriptional regulator that exists as a dimer and regulates transcription of genes
connected with SOS response in E . coli (Fernandez et al ., 2000). Under normal growth conditions, LexA
prevents transcription of genes under its control by binding to their promoter regions but during
SOS response the binding of RecA to the damaged DNA strand triggers autocleavage of LexA into
monomers that no longer can bind to its binding sites. Due to this, all such genes under the regulation
of LexA are induced and expressed in a co-ordinated manner (Michel, 2005). But the type of genes
regulated by LexA in different cyanobacteria has been found to be different. Studies conducted
on Synechocystis sp. strain PCC 6803 point out that LexA may regulate transcription of genes of
carbon metabolism (Domain et al ., 2004), bidirectional hydrogenase genes ( hoxEFUYH ; Gutekunst
et al ., 2005; Oliveira and Lindblad, 2005) and crhR gene that encodes a RNA helicase (Patterson-
Fortin et al ., 2008). The binding of LexA to a 14 bp pseudo-palindromic sequence in Anabaena sp.
strain PCC 7120 has been demonstrated (Mazon et al ., 2004). In this organism, the hoxEFUYH exists
as two operons, i.e. hoxEF and hoxUYH . Sjoholm et al . (2007) demonstrated that LexA regulates
transcription of these two operons by binding to the upstream of promoter regions of hoxE and
hoxU . In Synechocystis also a LexA-binding region consists of a 13 bp pesudo-palindromic segment
5'-AGTAACTAGTTCG-3' upstream of the promoter of hoxE (Gutekunst et al ., 2005). Li et al . (2010)
conducted a computational analysis of genes regulated by LexA in 33 cyanobacterial genomes. Six
of the cyanobacterial genomes ( G . violaceus PCC 7421, Synechococcus sp. JA-3-3-A'b, Synechococcus sp.
JA-2-3-3B'a (2-13), S . elongatus PCC 6301, S . elongatus PCC 7942, T . elongatus BP-1 and T . erythraeum
IMS101) do not possess a lexA gene. The SOS response in these strains is suspected to be regulated
by a transcriptional regulator other than LexA. The rest of the 27 genomes of cyanobacteria [ A .
marina MBIC11017, Anabaena sp. strain PCC 7120, A . variabilis ATCC 29413, Cyanothece sp. PCC 8801,
M . aeruginosa NIES-843, N . punctiforme PCC 73102, 12 strains of P . marinus (AS9601, CCMP1375,
MED4, MIT9211, MIT9215, MIT9301, MIT9303, MIT9312, MIT9313, MIT9515, NATL1A, NATL2A),
8 strains of Synechococcus sp. (CC9311, CC9605, CC9902, PCC 7002, RCC307, WH8102, WH7803 and
WH8102) and Synechocystis sp. strain PCC 6803] revealed the presence of lexA gene. According to
Li et al . (2010) LexA might still serve as a transcriptional regulator for the SOS response in many of
these cyanobacterial strains as LexA-binding sites of the core SOS-responsive genes recA and lexA
are the most conserved. However, the extent to which other SOS-responsive genes are regulated
is found to be different in these strains. For example, ruvB gene that encodes DNA helicase B has
the LexA-binding sites in the HL-adapted P . marinus strains (MIT9312, MIT9515, MIT9215, MED4
and AS9601). Of the four nucleotide excision repair genes uvrA , uvrB , uvrC and uvrD , known to be
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