Two mutations in the β-globin polyadenylylation signal reveal extended transcripts and new RNA polyadenylylation sites

Deborah Rund, Carol Dowling, Khamis Najjar, Eliezer A. Rachmilewitz, Haig Kazazian, Ariella Oppenheim

Research output: Contribution to journalArticle

Abstract

Two mutations in the β-globin poly(A) signal were identified in Israeli patients with β+-thalassemia by sequence analysis following PCR. One is a point mutation (AATAAA → AATAAG) and the other is a 5-base-pair deletion (AATAAA → A - ). The mutant genes were used to investigate the function of the poly(A) signal in vivo and to evaluate the mechanism whereby these mutations lead to a thalassemic phenotype. Analysis of RNA derived from peripheral blood demonstrated the presence of elongated RNA species in patients carrying either mutation. Other aspects of RNA processing (initiation, splicing) were unimpaired. RNA obtained from the patients carrying the point mutation contained four discrete, extended RNA species, 1500-2900 nucleotides long, which were found to be polyadenylylated. Some normal cleavage-polyadenylylation was also observed. The 5-base-pair deletion completely abolished cleavage at the normal site. This deletion mutation resulted in a phenotype of β+-thalassemia, thus providing evidence that the extended mRNAs are translatable in vivo. Furthermore, additional transcripts, >5 kilobases, presumably mRNA precursors, were found in all RNA samples, including those of nonthalassemic controls. The extended transcripts of the poly(A) mutants, together with the high molecular weight precursors, suggest that the human β-globin gene transcription unit is significantly longer than previously recognized..

Original languageEnglish (US)
Pages (from-to)4324-4328
Number of pages5
JournalProceedings of the National Academy of Sciences of the United States of America
Volume89
Issue number10
StatePublished - 1992

Fingerprint

Globins
RNA
Mutation
Poly A
Thalassemia
Point Mutation
Base Pairing
Phenotype
Sequence Deletion
RNA Precursors
Genes
Sequence Analysis
Nucleotides
Molecular Weight
Polymerase Chain Reaction
Messenger RNA

Keywords

  • β-thalassemia
  • Polymerase chain reaction
  • RNA processing

ASJC Scopus subject areas

  • Genetics
  • General

Cite this

Two mutations in the β-globin polyadenylylation signal reveal extended transcripts and new RNA polyadenylylation sites. / Rund, Deborah; Dowling, Carol; Najjar, Khamis; Rachmilewitz, Eliezer A.; Kazazian, Haig; Oppenheim, Ariella.

In: Proceedings of the National Academy of Sciences of the United States of America, Vol. 89, No. 10, 1992, p. 4324-4328.

Research output: Contribution to journalArticle

Rund, Deborah ; Dowling, Carol ; Najjar, Khamis ; Rachmilewitz, Eliezer A. ; Kazazian, Haig ; Oppenheim, Ariella. / Two mutations in the β-globin polyadenylylation signal reveal extended transcripts and new RNA polyadenylylation sites. In: Proceedings of the National Academy of Sciences of the United States of America. 1992 ; Vol. 89, No. 10. pp. 4324-4328.
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