How to find the promoter sequence of this gene - (May/23/2006 )
HI,How to find the promoter sequence and design the MSP primer of this gene?
The gene's name is IGSF4 OR TSLC1 ,I find the sequence of this gene from NCBI
      1 gacatggcga gtgtagtgct gccgagcgga tcccagtgtg cggcggcagc ggcggcggcg
       61 gcgcctcccg ggctccggct ccggcttctg ctgttgctct tctccgccgc ggcactgatc
      121 cccacaggtg atgggcagaa tctgtttacg aaagacgtga cagtgatcga gggagaggtt
      181 gcgaccatca gttgccaagt caataagagt gacgactctg tgattcagct actgaatccc
      241 aacaggcaga ccatttattt cagggacttc aggcctttga aggacagcag gtttcagttg
      301 ctgaattttt ctagcagtga actcaaagta tcattgacaa acgtctcaat ttctgatgaa
      361 ggaagatact tttgccagct ctataccgat cccccacagg aaagttacac caccatcaca
      421 gtcctggtcc caccacgtaa tctgatgatc gatatccaga gagacactgc ggtggaaggt
      481 gaggagattg aagtcaactg cactgctatg gccagcaagc cagccacgac tatcaggtgg
      541 ttcaaaggga acacagagct aaaaggcaaa tcggaggtgg aagagtggtc agacatgtac
      601 actgtgacca gtcagctgat gctgaaggtg cacaaggagg acgatggggt cccagtgatc
      661 tgccaggtgg agcaccctgc ggtcactgga aacctgcaga cccagcggta tctagaagta
      721 cagtataagc cacaagtgca cattcagatg acttatcctc tacaaggctt aacccgggaa
      781 ggggacgcgc ttgagttaac atgtgaagcc atcgggaagc cccagcctgt gatggtaact
      841 tgggtgagag tcgatgatga aatgcctcaa cacgccgtac tgtctgggcc caacctgttc
      901 atcaataacc taaacaaaac agataatggt acataccgct gtgaagcttc aaacatagtg
      961 gggaaagctc actcggatta tatgctgtat gtatacgatc cccccacaac tatccctcct
     1021 cccacaacaa ccaccaccac caccaccacc accaccacca ccatccttac catcatcaca
     1081 gattcccgag caggtgaaga aggctcgatc agggcagtgg atcatgccgt gatcggtggc
     1141 gtcgtggcgg tggtggtgtt cgccatgctg tgcttgctca tcattctggg gcgctatttt
     1201 gccagacata aaggtacata cttcactcat gaagccaaag gagccgatga cgcagcagac
     1261 gcagacacag ctataatcaa tgcagaagga ggacagaaca actccgaaga aaagaaagag
     1321 tacttcatct agatcagcct ttttgtttca atgaggtgtc caactggccc tatttagatg
     1381 ataaagagac agtgatattg gaacttgcga gaaattcgtg tgttttttta tgaatgggtg
     1441 gaaaggtgtg agactgggaa ggcttgggat ttgctgtgta aaaaaaaaaa aaaatgttct
     1501 ttggaaagta cactctgctg tttgacacct cttttttcgt ttgtttgttt gtttaatttt
     1561 tatttcttcc taccaagtca aacttggata cttggattta gtttcagtag attgcagaaa
     1621 attctgtgcc ttgttttttg tttgtttgtt gcgttccttt cttttccccc tttgtgcaca
     1681 tttatttcct ccctctaccc caatttcgga ttttttccaa aatctcccat tttggaattt
     1741 gcctgctggg attccttaga ctcttttcct tcccttttct gttctagttt tttacttttg
     1801 tttattttta tggtaactgc tttctgttcc aaattcagtt tcataaaagg agaaccagca
     1861 cagcttagga tttcatagtt cagaatttag tgtatccata atgcattctt ctctgttgtc
     1921 gtaaagattt gggtgaacaa acaatgaaaa ctctttgctg ctgcccatgt ttcaaatact
     1981 tagagcagtg aagactagaa aattagactg tgattcagaa aatgttctgt ttgctgtgga
     2041 actacattac tgtacagggt tatctgcaag tgaggtgtgt cacaatgaga ttgaatttca
     2101 ctgtctttaa ttctgtatct gtagacggct cagtatagat accctacgct gtccagaaag
     2161 gtttggggca gaaaggactc ctcctttttc catgccctaa acagacctga caggtgaggt
     2221 ctgttccttt tatataagtg gacaaatttt gagttgccac aggaggggaa gtagggaggg
     2281 gggaaataca gttctgctct ggttgtttct gttccaaatg attccatcca cctttcccaa
     2341 tcggccttac ttctcactaa tttgtaggaa aaagcaagtt cgtctgttgt gcgaatgact
     2401 gaatgggaca gagttgattt tttttttttt tttcctttgt gcttagttag gaaggcagta
     2461 ggatgtggcc tgcatgtact gtatattaca gatatttgtc atgctgggat ttccaactcg
     2521 aatctgtgtg aaactttcat tccttcagat ttggcttgac aaaggcagga ggtacaaaag
     2581 aagggctggt attgttctca cactggtctg ctgtcgctct cagttctcga taggtcagag
     2641 cagaggtgga aaaacagcat gtacggattt tcagttactt aatcaaaact caaatgtgag
     2701 tgtttttatc tttttacctt tcatacacta gccttggcct ctttcctcag ccttaagaac
     2761 catctgccaa aaattactga tcctcgcatg atggcagcca tagtgcatag ctactaaaat
     2821 cagtgacctt gaacatatct tagatgggga gcctcgggaa aaggtagagg agtcacgtta
     2881 ccatttacat gttttaaaga aagaagtgtg gggattttca ctgaaacgtc taggaaatct
     2941 agaagtagtc ctgaaggaca gaaactaaac tcttaccata tgtttggtaa gactccagac
     3001 tccagctaac agtccctatg gaaagatggc atcaaaaaag atagatctat atatatatat
     3061 aaatatatat tctattacat tttcagtgag taattttgga ttttgcaagg tgcattttta
     3121 ctattgttac attatgtgga aaacttatgc tgatttattt aagggggaaa aagtgtcaac
     3181 tctttgttat ttgaaaacat gtttattttt cttgtcttta ttttaacctt tgatagaacc
     3241 attgcaatat gggggccttt tgggaacgga ctggtatgta aaagaaaatc cattatcgag
     3301 cagcatttta tttacccctc ccctatccct aggcacttaa ccaagacaaa aagccacaat
     3361 gaacatccct ttttcaatga attttataat ctgcagctct attccgagcc cttagcaccc
     3421 attccgacca tagtataatc atatcaaagg gtgagaatca tttagcatgt tgttgaaagg
     3481 ttttttttca gttgttcttt ttagaaaaaa ag
 
                                                                            THANKS
had a quick look at your gene in genome browser and (see attached) there is a CpG island at the 5' end of this gene which could be a part of the promoter. Just click on the green CpG island and it will pull up the sequenc from which you can design assays for
Good luck!
Nick
Here is the actual promoter sequence (1kb upstream). Sequence highlighted is the first exon.
GAAGGGCTGGGGGCGCAGAGGAGGAGTGAGAGGGTTTGAGCCCCGAAGGAGGAACACGGC
AGACCCTGCCTTCACCACACTCCCTCTCCCCAACTCCCACCACCCCCGCTCTTCACCTGA  
AGCCTTGACTAATTTTTTCCGTTGTTGTGTAATCTTAAATATCTAATATTACAAATATTT  
CACACATATATTCAACACACACCTATATATTAAAACCAGGGAGGAGACCCTCGACAAGCG  
GAGGAGCCTGAGCATACCCTCCTCGATCTACCTTTCCCGAGATTCTGCCGCAAAAAGACC  
GACTGGAAAATCTCAGAACCCGACTCTACGGCTGCCTTCTCCAACTATCCCCGAGTCTAC  
CGCTAGGCTGTTGAGCGGGCTCTCCCGCTCCGCCGGACGTGCAAAGCACGCATGCACTTC  
TCCCAGATTGTTTTGTCAATCCGGGGACCTGCCTTCTTACTCTCCACTCCCGCACAGCCC  
CCGTTCCCAAAGATCTATTCCTTCGGTGCAAGGTGAGTGACGGAAATTTGCAACGTCTGG  
TTCGCTAGGCCAGATGCACTCGGTGTGCGGGACAGAGGACCCTCTTAAGGGAGATTCTCC  
AGTCGTCGGTCTGATACAGCGATTGCTATAAACATTCCTAATAAAGGTGTACAAGAAGCT  
AGACCCGCCCCCTGGAGCCCGAGTCCTTGCACGCCAGGCGCCCGGGAGAACACTTTTTCC  
TTGATCCGGGGAAAGCAAAACCCGAATTTTAACATAAACATATTTGCATACGCCCCTCCC  
CTTGGCCCCGCCCCTAGGTGGCGCGGGCGCGCCGCCGAACGCCAGCGCCAGGGGGCGGGG  
TGGGGGAGGGAGCGAGGCCCTCCGAGAGCCGGGTTGGGCTCGCGGCGCTGTGATTGGTCT  
GCCCGGACTCCGCCTCCAGCGCATGTCATTAGCATCTCATTAGCTGTCCGCTCGGGCTCC  
GGAGGCAGCCAACGCCGCCAGTCTGAGGCAGGTGCCCGACATGGCGAGTGTAGTGCTGCC  
GAGCGGATCCCAGTGTGCGGCGGCAGCGGCGGCGGCGGCGCCTCCCGGGCTCCGGCTCCG  
GCTTCTGCTGTTGCTCTTCTCCGCCGCGGCACTGATCCCCACAGGTAGGTGTGGGCACCG
Usually, you find out the ATG of the first exon and then consider the 1kb or even 2kb upstream region would contain promoter of that gene. I know once study on GPCRs where they considered 5kb region
Thank you very much!
 
Hi PCRMAN
     I  Have the same question,my gene name is stathmin.    Waiting for your reply,THANKS 
         1 atcaccgggc gtccgctccg gggtgccgtc gaggagacaa tagggggcgt gggccctcgt
       61 ttacctccct ccctccctcc cttccctgcg ggccccgccg ggttccccat tgtctgaagg
      121 gacggggcgg tgccccaggg accagcggct ttaggaccaa actgcgggca gccagggccg
      181 cgaccctccc tgcgaccgtc ccctggcgac cgcagctggt gattgagggg cggcgctccc
      241 gggccccacg agggttcttc tgtcttcgcg gccggacgcg cggacagcgt gggtggcggc
      301 aggactttcc ttatcccagt tgattgtgca gaatacactg cctgtcgctt gtcttctatt
      361 caccatggct tcttctgata tccaggtgaa agaactggag aagcgtgcct caggccaggc
      421 ttttgagctg attctcagcc ctcggtcaaa agaatctgtt ccagaattcc ccctttcccc
      481 tccaaagaag aaggatcttt ccctggagga aattcagaag aaattagaag ctgcagaaga
      541 aagacgcaag tcccatgaag ctgaggtctt gaagcagctg gctgagaaac gagagcacga
      601 gaaagaagtg cttcagaagg caatagaaga gaacaacaac ttcagtaaaa tggcagaaga
      661 gaaactgacc cacaaaatgg aagctaataa agagaaccga gaggcacaaa tggctgccaa
      721 actggaacgt ttgcgagaga aggataagca cattgaagaa gtgcggaaga acaaagaatc
      781 caaagaccct gctgacgaga ctgaagctga ctaatttgtt ctgagaactg actttctccc
      841 catccccttc ctaaatatcc aaagactgta ctggccagtg tcattttatt ttttccctcc
      901 tgacaaatat tttagaagct aatgtaggac tgtataggta gatccagatc cagactgtaa
      961 gatgttgttt taggggctaa aggggagaaa ctgaaagtgt tttactcttt ttctaaagtg
     1021 ttggtctttc taatgtagct atttttcttg ttgcatcttt tctacttcag tacacttggt
     1081 gtactgggtt aatggctagt actgtattgg ctctgtgaaa acatatttgt gaaaagagta
     1141 tgtagtggct tcttttgaac tgttagatgc tgaatatctg ttcacttttc aatcccaatt
     1201 ctgtcccaat cttaccagat gctactggac ttgaatggtt aataaaactg cacagtgctg
     1261 ttggtggcag tgacttcttt tgagttaggt taataaatca agccatagag cccctcctgg
     1321 ttgatacttg ttccagatgg ggcctttggg gctggtagaa atacccaacg cacaaatgac
     1381 cgcacgttct ctgccccgtt tcttgcccca gtgtggtttg cattgtctcc ttccacaatg
     1441 actgctttgt ttggatgcct cagcccaggt cagctgttac tttctttcag atgtttattt
     1501 gcaaacaacc attttttgtt ctgtgtccct tttaaaaggc agattaaaag cacaagcgtg
     1561 tttctagaga acagttgaga gagaatctca agattctact tggtggtttg cttgctctac
     1621 gttacaggtg gggcatgtcc tcatcctttc ctgccataaa agctatgaca cgagaatcag
     1681 aatattaata aaactttatg tactgctgta gcaaaaaaaa aaaaaaaaaa
pcrman: what if there more than one ATG ...
how could you know the first promotor?
Jiang M: how to determine the size of your promotor?
STMN1 5'-flanking region (the first 1kb).
TCAGTATCTGAATTATTCCTGGTCCTGCTCACAGGCTAAGTGAAAACCACTTCGATTGGC
TTGGGGGGGAGGCCGACCCCACACAAGGGCGATTGTTGGAAAAAATGCCGCAACAAGCAT
ATTTCAGGCAACAGCGCATTGCTAATTGTTTGCTTTGTGTAGTGTGCTGCTGCTTGTATG
ATCCAGTTTTTATTGTCTTGGGCACCCCTTAGTTGTATTTTATCTCTGGCACATCCCTGG
TGACTAACTAGGCATGAGAGTCTTTCTAAATTAGGACTGTTGTTTCAGGAAGGTTGGTCA
CATTTGTTTCTTGATTTGGGGAGATGCAGCTCATTAATAAAATAAAGATATCTCTTCTGC
TTAGTCAAGATCTCAAAGCAGGTGTCTTGGTGTATTGACCACCAACCGAGGACACGGTCT
TGGTCAGAGAATGGGAGGAGGCGGGGACCATGTTCATTTCATTTATTTTTTTCCCCTTTT
TGTGAGAGAAAGGGCCAGTTATTCTAAGGCACGGTCAGACCAATTTCCTTTGTGCCTTTG
CTGAGGTTCTGAGCTATCCAGGTCAGGGAGAACAGTGACCTTGTGGCTCCTTTTTCGATT
TTTAAAAAGAACCCAGTGCTGCTCTGGGGAGCACGTGCTCTGAGAACAAAAGCAACACTT
AACTGCAATCTGTGTAGTCTAGAACGGCTATTGCTCTTCCTCCCCTATCATCCGCAGAAG
GCTTGGAAGAACAGATGGAGTCTGCATTTAAGCTGAGTGGCTTTGTTAGACCAAAGGCGA
TCAAATTCCAGAGCCCCACGCTTTCCCGCACAGGTCCCTGGTCACCGGCTCGGGAACCTG
AGGATGCTGGCAAGAACGCACACAGTGAGGGAAGGGCCACGCCCGCGACCTGTGGGCTGA
GTGGATTAGAAATTACGATGATGTCACAATATGGGTGACACGCCGGTGTCGGTGTAGGGT
GCCGGGGGCAGGGGGCCCTGCAGGGGCGTGGAGTGGCATTGTGCTGTCACAGGGGCTCGG
GCGTCTTAGGCACCCATGTGGGTGGCGCACTAGAAGGGGCACTGCTCTGTCCGAGTGCTG
CCCTTGGGGCGAGGCGGGCATGTGGCTCTACAAGGTGGAGTCCAGGCGGCCAAAGTTTGG AAAG
how could you know the first promotor?
Jiang M: how to determine the size of your promotor?
Ideally, promoter has to be determined experimentally by reporter gene analysis for example. Since most promoters lie immediately upstream transcription start site (first exon), the 5' flanking sequence of the first exon highly likely contains the promoter especially if it also contains CpG islands. If different transcript isoforms use alternative promoters, it is hard to pinpoint the promoter by database search.
can we estimate/guess  the position of a promoter theoretically?
i mean without using databases, softwares....
