SMART amplification combined with cDNA size fractionation in order to obtain large full-length clones

BMC Genomics. 2004 Jun 15;5(1):36. doi: 10.1186/1471-2164-5-36.

Abstract

Background: cDNA libraries are widely used to identify genes and splice variants, and as a physical resource for full-length clones. Conventionally-generated cDNA libraries contain a high percentage of 5'-truncated clones. Current library construction methods that enrich for full-length mRNA are laborious, and involve several enzymatic steps performed on mRNA, which renders them sensitive to RNA degradation. The SMART technique for full-length enrichment is robust but results in limited cDNA insert size of the library.

Results: We describe a method to construct SMART full-length enriched cDNA libraries with large insert sizes. Sub-libraries were generated from size-fractionated cDNA with an average insert size of up to seven kb. The percentage of full-length clones was calculated for different size ranges from BLAST results of over 12,000 5'ESTs.

Conclusions: The presented technique is suitable to generate full-length enriched cDNA libraries with large average insert sizes in a straightforward and robust way. The representation of full-coding clones is high also for large cDNAs (70%, 4-10 kb), when high-quality starting mRNA is used.

MeSH terms

  • Cell Line, Tumor
  • Cloning, Molecular / methods
  • DNA, Complementary / chemistry
  • DNA, Complementary / genetics*
  • DNA, Complementary / metabolism*
  • DNA, Neoplasm / chemistry
  • DNA, Neoplasm / genetics
  • DNA, Neoplasm / metabolism
  • Electrophoresis, Agar Gel / methods
  • Endometrial Neoplasms / genetics
  • Endometrial Neoplasms / pathology
  • Female
  • Gene Library
  • Humans
  • Nucleic Acid Amplification Techniques / methods*
  • RNA, Messenger / genetics
  • RNA, Neoplasm / genetics
  • Reverse Transcriptase Polymerase Chain Reaction / methods*

Substances

  • DNA, Complementary
  • DNA, Neoplasm
  • RNA, Messenger
  • RNA, Neoplasm