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The ftsZ Gene of Mycobacterium smegmatis is expressed Through Multiple Transcripts
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The principal essential bacterial cell division gene
ftsZ
is differentially expressed through multiple transcripts in diverse genera of bacteria in order to meet cell division requirements in compliance with the physiological niche of the organism under different environmental conditions. We initiated transcriptional analyses of
ftsZ
gene of the fast growing saprophytic mycobacterium,
Mycobacterium smegmatis
, as the first step towards understanding the requirements for FtsZ for cell division under different growth phases and stress conditions. Primer extension analyses identified four transcripts, T1, T2, T3, and T4. Transcriptional fusion studies using
gfp
showed that the respective putative promoter regions, P1, P2, P3, and P4, possessed promoter activity. T1, T2, and T3 were found to originate from the intergenic region between
ftsZ
and the upstream gene,
ftsQ
. T4 was initiated from the 3’ portion of the open reading frame of
ftsQ
. RT-PCR analyses indicated co-transcription of
ftsQ
and
ftsZ
. The four transcripts were present in the cells at all growth phases and at different levels in the cells exposed to a variety of stress conditions
in vitro
. T2 and T3 were absent under hypoxia and nutrient-depleted stationary phase conditions, while the levels of T1 and T4 remained unaffected. These studies showed that
ftsZ
gene expression through multiple transcripts and differential expression of the transcripts at different growth phases and under stress conditions are conserved in
M. smegmatis
, like in other
Actinomycetes
.
Bentham Science Publishers Ltd.
Title: The ftsZ Gene of Mycobacterium smegmatis is expressed Through Multiple Transcripts
Description:
The principal essential bacterial cell division gene
ftsZ
is differentially expressed through multiple transcripts in diverse genera of bacteria in order to meet cell division requirements in compliance with the physiological niche of the organism under different environmental conditions.
We initiated transcriptional analyses of
ftsZ
gene of the fast growing saprophytic mycobacterium,
Mycobacterium smegmatis
, as the first step towards understanding the requirements for FtsZ for cell division under different growth phases and stress conditions.
Primer extension analyses identified four transcripts, T1, T2, T3, and T4.
Transcriptional fusion studies using
gfp
showed that the respective putative promoter regions, P1, P2, P3, and P4, possessed promoter activity.
T1, T2, and T3 were found to originate from the intergenic region between
ftsZ
and the upstream gene,
ftsQ
.
T4 was initiated from the 3’ portion of the open reading frame of
ftsQ
.
RT-PCR analyses indicated co-transcription of
ftsQ
and
ftsZ
.
The four transcripts were present in the cells at all growth phases and at different levels in the cells exposed to a variety of stress conditions
in vitro
.
T2 and T3 were absent under hypoxia and nutrient-depleted stationary phase conditions, while the levels of T1 and T4 remained unaffected.
These studies showed that
ftsZ
gene expression through multiple transcripts and differential expression of the transcripts at different growth phases and under stress conditions are conserved in
M.
smegmatis
, like in other
Actinomycetes
.
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