A functional component of the sea urchin H2A gene modulator contains an extended sequence homology to a viral enhancer
Author(s) -
Rudolf Grosschedl,
Marco Mächler,
Urs Hoffmann Rohrer,
Max L. Birnstiel
Publication year - 1983
Publication title -
nucleic acids research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 9.008
H-Index - 537
eISSN - 1362-4954
pISSN - 0305-1048
DOI - 10.1093/nar/11.23.8123
Subject(s) - biology , enhancer , gene , transcription (linguistics) , dna , microbiology and biotechnology , homology (biology) , genetics , sequence analysis , gene expression , linguistics , philosophy
The DNA sequences imparting a maximal rate of sea urchin H2A gene transcription in the frog oocyte nucleus were narrowed down by deletion mapping to a DNA segment -165 to -111, far-upstream of the H2A mRNA cap site. C to T base changes in this area create strong down mutations, hence the primary structure of this DNA sequence is of paramount importance to the H2A gene expression. Sequence comparisons suggest that the -165 to -111 region may contain two essential sequence blocks. Most strikingly, the -135 area contains a 14 out of 17 basepair homology to the Moloney murine sarcoma virus enhancer and to topologically related 5' LTR-sequences of the simian sarcoma virus and the murine Friend spleen focus forming virus.
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