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  • Technician
  • Undergraduate Student
  • Veterinary
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  • Deputy Director of Center
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  • Deputy Head of Facility
  • Director of Center
  • Director of Department
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© Research
Publication : Biochemistry

Properties of human liver cytosolic aspartate aminotransferase mRNAs generated by alternative polyadenylation site selection

Scientific Fields
Diseases
Organisms
Applications
Technique

Published in Biochemistry - 05 Jun 1990

Bousquet-Lemercier B, Pol S, Pavé-Preux M, Hanoune J, Barouki R

Link to Pubmed [PMID] – 1974457

Biochemistry 1990 Jun;29(22):5293-9

Human cytosolic aspartate aminotransferase (cAspAT) cDNA clones have been isolated from an adult human liver cDNA library. Among the clones, two cDNAs of 1550 and 1950 base pairs, respectively, have been characterized. These two cDNAs differ only in the lengths of their 3′ noncoding regions and by the presence of one or two putative polyadenylation signals AATAAA. Northern blot analysis revealed two different mRNAs of 2.1 and 1.8 kbp in several human tissues, whereas Southern blot analysis suggested the existence of a single gene for the human cAspAT. The two mRNA species result from the alternative use of two polyadenylation signals. In the liver, the relative ratio of these mRNAs varies among different species and, in humans at least, during development. The properties of the two mRNAs were compared. The half-lives of the 2.1 and 1.8 kbp mRNAs, in the HepG2 cell line, are 8 and 12 h, respectively. The two mRNAs have similar and rather short poly(A) tracts of 20-50 nucleotides. Both mRNAs are capable of directing the in vitro synthesis of the cAspAT protein. We conclude that both the 2.1 and 1.8 kbp cAspAT mRNAs are functional and exhibit similar properties.