TRANSLATION INITIATION FACTOR-EIF-2 - CLONING AND EXPRESSION OF THE HUMAN CDNA-ENCODING THE GAMMA-SUBUNIT

被引:0
作者
GASPAR, NJ
KINZY, TG
SCHERER, BJ
HUMBELIN, M
HERSHEY, JWB
MERRICK, WC
机构
[1] UNIV CALIF DAVIS,SCH MED,DEPT BIOL CHEM,DAVIS,CA 95616
[2] CASE WESTERN RESERVE UNIV,SCH MED,DEPT BIOCHEM,CLEVELAND,OH 44106
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中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Translation initiation factor eIF-2 is a heterotrimeric GTP-binding protein involved in the recruitment of methionyl-tRNA(i) to the 40 S ribosomal subunit. To complete our characterization of eIF-2, we cloned and characterized a human cDNA encoding the largest subunit, eIF-2gamma. From limited peptide sequence data, degenerate oligonucleotide primers were designed to amplify-a 118-base pair DNA fragment from a cDNA library. This fragment was used as a probe to screen for larger cDNAs and eventually a clone containing the complete eIF-2gamma coding region (1416 base pairs) was identified. It encodes a 472-amino acid protein (51.8 kDa) and contains the three consensus GTP-binding elements. The protein shares strong homology to EF-Tu, GCD11 (the yeast homolog of eIF-2gamma), and other EF-Tu-like proteins. Transfection of COS-1 cells with the cDNA results in overexpression of a 52-kDa protein which is specifically recognized by anti-eIF-2gamma antibodies. Cross-linking experiments with diepoxybutane and trans-diaminedichloroplatinum(II) indicate that both the beta- and gamma-subunits of eIF-2 are in close proximity to methionyl-tRNA(i) in ternary complexes. Possession of the eIF-2gamma cDNA will facilitate future investigations of the interactions of GTP and methionyl-tRNA(i) with eIF-2.
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页码:3415 / 3422
页数:8
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