ALTERNATIVE PROCESSING OF MESSENGER-RNAS ENCODING MAMMALIAN CHROMOSOMAL HIGH-MOBILITY-GROUP PROTEINS HMG-I AND HMG-Y
ALTERNATIVE PROCESSING OF MESSENGER-RNAS ENCODING MAMMALIAN CHROMOSOMAL HIGH-MOBILITY-GROUP PROTEINS HMG-I AND HMG-Y
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DOI:
10.1128/mcb.9.5.2114
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发表时间:
1989-05-01
影响因子:
5.3
通讯作者:
REEVES, R
中科院分区:
文献类型:
--
作者:
JOHNSON, KR;LEHN, DA;REEVES, R
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 .cntdot. T-rich regions of DNA in vitro, and has been localized to particular regions of mammalian metaphase chromosomes. We isolated eight cDNA clones encoding HMG-1 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 36-base-pair in-frame deletion in their open reading frame (ORF); we found that this shortened ORF encodes the HMG-Y protein isoform. We present evidence tha 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-I or HMG-Y gene copies exist in the human genome; we isolated and partially sequenced one of these pseudogenes and found that it is a processed HMG-Y retropseudogene.