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Alternative processing of mRNAs encoding mammalian chromosomal high-mobility-group proteins HMG-I and HMG-Y

Journal Article · · Mol. Cell. Biol.; (United States)
DOI:https://doi.org/10.1128/MCB.9.5.2114· OSTI ID:5604354
The high-mobility-group protein HMG-I is a well-characterized nonhistone chromosomal protein that is preferentially expressed in rapidly dividing cells, binds to A . T-rich regions of DNA in vitro, and has been localized to particular regions of mammalian metaphase chromosomes. The authors isolated eight cDNA clones encoding HMG-I and its isoform HMG-Y from a human Raji cell cDNA library and detected blocks of nucleotide sequence rearrangements in the 5'-untranslated regions of these clones. In addition to this leader sequence variation, five of the eight cDNA clones had either a 33- or 3-base-pair in-frame deletion in their open reading frame (ORF); the author found that this shortened ORF encodes the HMG-Y protein isoform. They present evidence that the 5'-untranslated-region and ORF heterogeneity of the cDNA clones is the result of alternative processing of RNA transcripts from a single functional gene. Several additional but probably nonfunctional HMG-1 or HMG-Y gene copies exist in the human genome; they isolated and partially sequenced one of these pseudogenes and found that is a processed HMG-Y retropseudogene.
Research Organization:
Washington State Univ., Pullman, WA (USA). Dept. of Biochemistry and Biophysics
OSTI ID:
5604354
Journal Information:
Mol. Cell. Biol.; (United States), Journal Name: Mol. Cell. Biol.; (United States) Vol. 9:5; ISSN MCEBD
Country of Publication:
United States
Language:
English