Seqanswers Leaderboard Ad

Collapse

Announcement

Collapse
No announcement yet.
X
 
  • Filter
  • Time
  • Show
Clear All
new posts

  • total RNA isolation: miRNeasy kit vs trizol

    I am isolating total RNA from a small number of drosophila heads (20) for diff gene expression analysis on NextSeq500. My goal is to generate two separate libraries from the samples: 1) coding RNA via poly(A) selection from total RNA and 2) small RNA library (<200 nt). I tried using the miRNesy micro kit from Qiagen (which in theory, allows for separation of a small [<200 nt] and large [>200 nt] fraction) however, I kept getting rRNA in my small RNA fraction and low yield in the large fraction. Qiagen was not helpful in trouble shooting so I moved away from kits entirely and have been optimizing isolating RNA from heads by trizol/chloroform with in solution DNAse digestion.

    Total RNA isolated by trizol/chloroform+ DNAse digestion has been QC'd via bioanalyzer and the gel and it appears there is no degradation of rRNA so I'm fairly comfortable moving forward with using trizol-extracted RNA for my poly-A(+) library prep. Any reason to think my sample might not be pure? Any concerns with not using column based?

    Found this paper Sultan, M. et al. Influence of RNA extraction methods and library selection schemes on RNA-seq data. BMC Genomics 15, 675 (2014). which makes it seem like trizol/chloroform is comparable to Qiagen columns.

    Thanks!

  • #2
    There is no particular issue using Trizol. You should check 260/230 and 260/280 ratios to ensure purity.

    Most of small RNA-seq library prep kits can use total RNA as input (prefered input) so there is no need to isolate small RNA.

    Comment


    • #3
      Just be aware that in drosophila, 2S RNA is abundant and 30nt long.
      You may (will?) need a specific protocol to build smallRNAseq libraries from drosophila RNA.

      Comment


      • #4
        Originally posted by huguesparri View Post
        Just be aware that in drosophila, 2S RNA is abundant and 30nt long.
        You may (will?) need a specific protocol to build smallRNAseq libraries from drosophila RNA.
        This is VERY important. We did a miRNA-Seq project for a client from Drosophila and were not aware of this fact. Output reads were 70-90% 2S rRNA depending on library. There is a specific protocol which uses a blocking oligo to prevent reverse transcription of the 2S rRNA. We have not tested this in our lab so cannot give any advice or insight as to how well it works.

        Comment


        • #5
          Thank you all! I was planning on isolating the relevant small RNAs from total RNA by gel but wasn't aware that the 2S unit migrated so closely to miRNA/piRNA. Will check out the protocol, thanks!

          Comment


          • #6
            Just a quick follow up - I am NOT doing a separate column based clean up of the total RNA isolated by trizol/chloroform. Because I am using so little starting material (20 fly heads) - the column just diminishes my RNA yield. Any concern? Thanks!

            Comment

            Latest Articles

            Collapse

            • seqadmin
              Essential Discoveries and Tools in Epitranscriptomics
              by seqadmin


              The field of epigenetics has traditionally concentrated more on DNA and how changes like methylation and phosphorylation of histones impact gene expression and regulation. However, our increased understanding of RNA modifications and their importance in cellular processes has led to a rise in epitranscriptomics research. “Epitranscriptomics brings together the concepts of epigenetics and gene expression,” explained Adrien Leger, PhD, Principal Research Scientist on Modified Bases...
              Yesterday, 07:01 AM
            • seqadmin
              Current Approaches to Protein Sequencing
              by seqadmin


              Proteins are often described as the workhorses of the cell, and identifying their sequences is key to understanding their role in biological processes and disease. Currently, the most common technique used to determine protein sequences is mass spectrometry. While still a valuable tool, mass spectrometry faces several limitations and requires a highly experienced scientist familiar with the equipment to operate it. Additionally, other proteomic methods, like affinity assays, are constrained...
              04-04-2024, 04:25 PM

            ad_right_rmr

            Collapse

            News

            Collapse

            Topics Statistics Last Post
            Started by seqadmin, 04-11-2024, 12:08 PM
            0 responses
            39 views
            0 likes
            Last Post seqadmin  
            Started by seqadmin, 04-10-2024, 10:19 PM
            0 responses
            41 views
            0 likes
            Last Post seqadmin  
            Started by seqadmin, 04-10-2024, 09:21 AM
            0 responses
            35 views
            0 likes
            Last Post seqadmin  
            Started by seqadmin, 04-04-2024, 09:00 AM
            0 responses
            55 views
            0 likes
            Last Post seqadmin  
            Working...
            X