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  • sindrle
    Senior Member
    • Aug 2013
    • 266

    #1

    Predicted Ensembl genes, but not in RefSeq

    Im curious, I find a lot of reads mapped to "Gm" annotated genes from Ensembl, which are predicted genes.

    When Im mapping to the UCSC genome (with novel discovery) I don't find anything..

    Could someone shed light on this? And is the "Gm" genes something to pursue?

    Im using Cufflinks-pipeline for this.
  • yueluo
    Member
    • Aug 2013
    • 82

    #2
    FYI, Ensembl tends to have many many more annotated genes/transcripts than UCSC/RefSeq. So I'd say it's quite normal if you can't find anything in UCSC.

    I'm not familiar with "Gm" genes though.

    Comment

    • mbblack
      Senior Member
      • Aug 2009
      • 245

      #3
      The convention by the International Nucleotide Sequence Database Collaboration is that the accession prefix "GM" is supposed to be used for EMBL nucleotide patent entries, so I am not clear as to just what annotation you used to map to.

      Where did you actually get your reference genome and annotation you used for the mapping run?

      I've never seen any predicted genes with that accession prefix in the Ensembl builds I've mapped to (Rat, not human in my case). I've always downloaded my mapping reference and annotation directly from Ensembl. Predicted genes use the standard "ENSRNOGxxx..." and transcripts use the standard "ENSRNOTxxx..." form and it is only in the annotation description that one can determine if it was a predicted entry or not. Those entries will show up in UCSC as predicted entries with their respective RefSeq predicted entry.
      Last edited by mbblack; 04-25-2014, 05:36 AM.
      Michael Black, Ph.D.
      ScitoVation LLC. RTP, N.C.

      Comment

      • sindrle
        Senior Member
        • Aug 2013
        • 266

        #4
        Im using Ensembl for mouse. But downloaded from iGenomes (made for Tophat2, via Illumina).

        Comment

        • WhatsOEver
          Senior Member
          • Apr 2012
          • 215

          #5
          I had similar "problems" using the human hg19 assembly from different sources, until I found this paper "Assessing the impact of human genome annotation choice on RNA-seq expression estimates" which scientifically supports yueluo's statement

          Comment

          • mbblack
            Senior Member
            • Aug 2009
            • 245

            #6
            Looking in the actual "Mus_musculus.GRCm38.75.gtf" file from Ensembl, yes in the descriptors there are Gmxxxxx accessions (but those are NOT Ensembl accessions).

            E.G. gene_id "ENSMUSG00000088333"; transcript_id "ENSMUST00000157708"; exon_number "1"; gene_name "Gm22848"; gene_source "ensembl"; gene_biotype "snRNA"; transcript_name "Gm22848-201"; transcript_source "ensembl"; exon_id "ENSMUSE00000846843";

            So, Gm22848 is actually a Flybase accession and those entries in Ensembl and Refseq will be handled on a case-by-case basis and manually curated, so some will not be in refseq at all, and those that are are likely to be provisional entries. Odds are any of those are pseudogenes in any mammal.

            Regardless, if you want to track those, I would not use the Flybase or any other associated meta-data with those entries. Use the actual Ensembl gene or transcript IDs and they should track through UCSC and NCBI data just fine. The match to Gmxxxxx is just the best available homology match, which happens to be Drosophila genes.

            A couple of others I quickly checked do have MGI entries, but they come up as not in the current assembly. But these are all from the HAVANA project (i.e. the Human and Vertebrate Analysis and Annotation team) so these entries are going to be problematic as they will be changing as evidence for those ORFs changes.

            P.S. bear in mind that the current Enzembl mouse build has 5935 pseudogenes (or putative pseudogenes) in it, and for many of those the annotation may be in flux and thus not necessarily synchronized across different databases. The same thing goes for the readthrough transcripts, which are also manually curated by the HAVANA team.
            Last edited by mbblack; 04-25-2014, 06:18 AM.
            Michael Black, Ph.D.
            ScitoVation LLC. RTP, N.C.

            Comment

            • sindrle
              Senior Member
              • Aug 2013
              • 266

              #7
              Great answer! Thank you!

              But, excuse my ignorance, what biological relevant questions might be answered by analysing the Ensembl Gm-genes. As you mentioned:

              E.G. gene_id "ENSMUSG00000088333"; transcript_id "ENSMUST00000157708"; exon_number "1"; gene_name "Gm22848"; gene_source "ensembl"; gene_biotype "snRNA"; transcript_name "Gm22848-201"; transcript_source "ensembl"; exon_id "ENSMUSE00000846843";

              Comment

              • mbblack
                Senior Member
                • Aug 2009
                • 245

                #8
                Oh, sorry. I should have added I would not waste time pursuing them. They mostly, if not exclusively, appear to be pseudogenes, so unless you are specifically interested in something about pseudogenes, I'd ignore them.

                That line was just a random one I pulled from the GTF file as an example - GTF file from here: http://uswest.ensembl.org/info/data/ftp/index.html
                Last edited by mbblack; 04-25-2014, 08:27 AM.
                Michael Black, Ph.D.
                ScitoVation LLC. RTP, N.C.

                Comment

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