The DOI matches its Crossref record; 27 of the 27 references it cites were found in a registry or an index.
Conserved features of eukaryotic hsp70 genes revealed by comparison with the nucleotide sequence of human hsp70.
Open accessAbstract
We have determined the nucleotide sequence of the human hsp70 gene and 5' flanking region. The hsp70 gene is transcribed as an uninterrupted primary transcript of 2440 nucleotides composed of a 5' noncoding leader sequence of 212 nucleotides, a 3' noncoding region of 242 nucleotides, and a continuous open reading frame of 1986 nucleotides that encodes a protein with predicted molecular mass of 69,800 daltons. Upstream of the 5' terminus are the canonical TATAAA box, the sequence ATTGG that corresponds in the inverted orientation to the CCAAT motif, and the dyad sequence CTGGAAT/ATTCCCG that shares homology in 12 of 14 positions with the consensus transcription regulatory sequence common to Drosophila heat shock genes. Comparison of the predicted amino acid sequences of human hsp70 with the published sequences of Drosophila hsp70 and Escherichia coli dnaK reveals that human hsp70 is 73% identical to Drosophila hsp70 and 47% identical to E. coli dnaK. Surprisingly, the nucleotide sequences of the human and Drosophila genes are 72% identical and human and E. coli genes are 50% identical, which is more highly conserved than necessary given the degeneracy of the genetic code. The lack of accumulated silent nucleotide substitutions leads us to propose that there may be additional information in the nucleotide sequence of the hsp70 gene or the corresponding mRNA that precludes the maximum divergence allowed in the silent codon positions.
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Cites
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CpG-rich islands and the function of DNA methylation
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Self-citationHuman major histocompatibility complex contains genes for the major heat shock protein HSP70.
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Human HSP70 promoter contains at least two distinct regulatory domains.
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Self-citationIntervening sequences increase efficiency of RNA 3' processing and accumulation of cytoplasmic RNA
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Metadata
- Authors
- Hunt, C., & Morimoto, R. I.
- Venue
- Proceedings of the National Academy of Sciences
- Published
- 1985-10
- Volume
- 82
- Issue
- 19
- Pages
- 6455-6459
- ISSN
- 0027-8424 (ISSN-L)
- 1091-6490
- OpenAlex
- W2055533988
- Cited by
- 855
- References
- 27
- FWCI
- 12.98
- Type
- journal article
- Language
- en
- Open access
- green
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