Identification Of An Intronic Enhancer Element
Diverse pro-inflammatory mediators (LPS, TNFa, IL-1b, IFN-g) regulate expression of MnSOD. To
comprehend the role of this anti-oxidant enzyme in cytoprotection,
we sought to further identify the critical DNA sequences which mediate
transcriptional regulation of this gene. In transfected
lung epithelial cells, a human growth hormone reporter gene system was utilized
to identify regulatory elements in the promoter and within a 6.1 kb internal
genomic fragment containing multiple DNase I
hypersensitive sites. Northern analysis revealed a 10-20 fold response to
pro-inflammatory mediators and inclusion of the internal fragment was
necessary to mimic these stimulus-dependent endogenous levels. The
inducible element was localized to a 260 bp fragment
in intron 2 coinciding with a previously defined DNase I hypersensitive site.


A comparison of the sequence in intron 2 from the rat and human genes as shown below
demonstrates a high degree of identity. The overall
homology between the two species being 60-65% within this intron.
rat (1) TTCTGGGAATAATTGTTTTAATGGCTAA-ACAAAATAGTATGCTGTCTTT
human (1) ---------TTAT-GTTTTAACGTTTTTTACAAAATAGTAT--TGTCTTT
Con
(1) T AT GTTTTAA G T ACAAAATAGTAT TGTCTTT
rat (50) TTAATCTATTAGTT-----TTT--ACAAGGAGAATAATTGTTAGCCGTGT
human (39) TTAATTTATTCGTTAGTGGTTTGCACAAGGAAGATAATCGATAGTCATGT
Con (51) TTAAT TATT GTT TTT
ACAAGGA ATAAT G TAG C TGT
rat (93) CTCTGGGT-TAGCTGTATTGCTTGAGAAAACCAGACAGTAAAA----TTC
human (89) TTTTTAGACTCTCTGTATTGCTTG-GTAAGCTACGTAGTAAAAAATGTTT
Cons (101) T T G T CTGTATTGCTTG G AA C
A AGTAAAA TT
rat (138) ACTTTTTCTTAAATACACTCTTATTGCCTCTCAGGTCTGGGAAACGGGTT
human(138) ACTTTTCCTTAAAT------GTTTTGAATTTCGGGGTTATGAAATTTGTT
Con (151) ACTTTT CTTAAAT T
TTG T TC GG T GAAA GTT
rat (188) GAGTAATTG-----------------GTTCACTGGGGGCATCTAGTGGAG
human(182) GAGTAATTTTTAGACAGTCACATCTTGTTGACTGGAGGCATCTAGTGGAA
Con (201)
GAGTAATT
GTT ACTGG GGCATCTAGTGGA
rat (221) AAGTGTGGTATTTTAGCATAGTTGTGT---AAGTGGCCCAACCAA-GAGA
human(232) AAATGCAGTATTTCAGCCTGATTGTGTTTGAAGTAAATGATTAAAAGAGG
Con (251) AA TG GTATTT AGC T TTGTGT
AAGT A AA GAG
rat (267) AGGAAATTACCACATTCTGGAAATTTTACTTGCAATAAGCAAATCACATA
human(282) AGGAAGTTACCACATTCTGGAAGATTTACTTGAGACAGAC--------GA
Con (301) AGGAA TTACCACATTCTGGAA TTTACTTG A A
C A
rat (317) ATCGTGAAT-ACGGGAAGAGACTC--TGATTTAGGAAATGACAGATTTGG
human(324) ACCTTGAATTACGGGAAAAGGCCCCGTGATTTAGGAAATAACAAATTTGG
Con (351) A C TGAAT ACGGGAA AG C C TGATTTAGGAAAT ACA ATTTGG
rat (364) GAAGGCTGTGGTAAT-AGTGAGTAGGGGAAAAGCCCAGTTGGGAAATCGT
human(374) GAAACATGTAATGGGGAGAGACT-GGGGAATACCCCAGTTGTGAAAGTAC
Con (401) GAA TGT T AG GA T
GGGGAA A CCCAGTTG GAAA
rat (413) TTCCTCTAAGGTGACATCTGACA------ACTTTCCTCTTAA-TGTTGTA
human(423) TTCCTGTAAGGCAACATCTGACACCAGGAACCTTTCTCTTCAGTATTTTA
Con (451) TTCCT TAAGG
ACATCTGACA AC TT CTCTT A T TT TA
rat (456) AAAACATGGTGATTTCAACCCTTCC---GTGGAGACAGAGCTGTATTTGT
human(473) AAAACAACTTAATTTCAGTCCTTTACTTGTGGAATCAGAGCCTTACTTAT
Con (501) AAAACA T ATTTCA
CCTT GTGGA CAGAGC TA TT T
rat (503) TTAGTGAATGCTGCTGGGAATAAGAAAGCCGTGGTTTTATTG-ACCTGGC
human(523) GTAATACAACCCACTGGAAAAAAGCTTTTTATTGTATTGTACTATATTGT
Con (551) TA T A C CTGG AA
AAG T GT TT T A T G
rat (552) TGAGGATGGATTTTGAAAAGGTGTTTACGTTTTATATTTCAG--------
human(573) TTATAAGTGATTGAGTACCTGCAGAGCTTTCTTTTACTTAAACATATTTT
Con (601) T A A GATT G A
G T TT TA TT
A
rat (594) --------------------------
human(623) AAAAATTATTAAAAAGATTTTCATGT
Con (651)
This element functions in an orientation- and position-independent manner as well as with a heterologous promoter, as shown below (left) utilizing the minimal viral thymidine kinase promoter. The ability to function with a heterologous promoter also satisfies the definition of a true enhancer. This figure also demonstrates that the homologous sequence within the human MnSOD exhibits identical enhancer activity. We have also placed the MnSOD enhancer/TK promoter in front of the DsRED reporter gene and as shown can generate red fluorescent cells in a stimulus specific manner. Another novel characteristic of this enhancer element involves its ability to support cytokine-inducible transcription in the absence of a classical promoter. Thus, we have identified a complex highly conserved, cytokine-responsive, intronic element within rat and human MnSOD which we describe as a prohancer.
Our current regulation efforts are focused on the cloning of a number of these
cognate trans-acting factors along with dominant negative experiments to
demonstrate physiological relevance for these protein-DNA contacts. We are also
currently using in vivo footprinting to detect
the stimulus-specific proteins associated with the intronic
enhancer element. A model illustrating a potential mechanism for the action of
an internal enhancer element is shown below.