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cDNA of a novel mRNA expressed predominantly in mouse kidney.

Abstract
We examined embryonic carcinoma (EC) cells for a potential prototype molecule of C3, the third component of complement. PCR primers, corresponding to the base sequence derived from the C3 cDNA of several species, were used for PCR amplification of the EC cell cDNA. All the PCR products obtained had the same sequence and showed no sequence homology to C3. Subsequently, cDNA clones were isolated from a mouse liver cDNA library using the PCR product as a probe. Unexpectedly, neither the base sequence of the cDNA clones nor the amino acid sequence deduced from the cDNA showed homology to C3, although partial homology was observed to a number of sequences from EST databases. We designated this new clone NCU-G1. Northern hybridization experiments revealed that NCU-G1 is expressed constitutively not only in the mouse fetus but also in various mouse tissues, and is most abundant in the kidney cortex.
AuthorsT Kawamura, N Kuroda, Y Kimura, E Lazoura, N Okada, H Okada
JournalBiochemical genetics (Biochem Genet) Vol. 39 Issue 1-2 Pg. 33-42 (Feb 2001) ISSN: 0006-2928 [Print] United States
PMID11444019 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Complement C3
  • DNA Primers
  • DNA, Complementary
  • Membrane Proteins
  • RNA, Messenger
Topics
  • Amino Acid Sequence
  • Animals
  • Base Sequence
  • Blotting, Northern
  • Cloning, Molecular
  • Complement C3 (genetics)
  • DNA Primers (chemistry)
  • DNA, Complementary (analysis)
  • Kidney (chemistry)
  • Membrane Proteins (genetics, metabolism)
  • Mice
  • Molecular Sequence Data
  • RNA, Messenger (genetics, metabolism)
  • Reverse Transcriptase Polymerase Chain Reaction
  • Sequence Homology, Amino Acid

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