Domanico S Z, DeNagel D C, Dahlseid J N, Green J M, Pierce S K
Department of Biochemistry, Molecular Biology and Cell Biology, Northwestern University, Evanston, Illinois 60208-3500.
Mol Cell Biol. 1993 Jun;13(6):3598-610. doi: 10.1128/mcb.13.6.3598-3610.1993.
We have previously described peptide-binding proteins of 72 and 74 kDa (PBP72/74), which have been implicated as playing a role in antigen processing and are serologically related to the 70-kDa heat shock protein (hsp70) family. Here we report the cloning and sequencing of the cDNA encoding PBP74 in mice and in humans, accomplished by using amino acid sequence information obtained from the purified protein. We show that PBP74 is highly homologous to members of the hsp70 family but, significantly, is not identical to any known member of this family. Inspection of the cDNA nucleotide sequence indicates that it encodes a 46-residue N-terminal peptide which is not present in the mature protein. Transcription and translation in vitro of the PBP74 cDNA verified that it encodes a form of PBP74 which is larger than the mature protein. The presequence does not conform to known motifs for organelle-targeting sequences, and at present, its function is not known. By confocal microscopy, PBP74 was localized to cytoplasmic vesicles but not to the nucleus, mitochondria, or plasma membrane by using antibodies specific for the N-terminal 16 residues of PBP74. By RNA filter hybridization analysis, PBP74 mRNAs are detected in all cell types tested. Exposure of cells to heat shock does not result in an increase in the mRNA levels of PBP74, unlike the dramatic increase observed for the stress-inducible hsp70 mRNA. Thus, PBP74 appears to be a constitutive, new member of the hsp70 family.
我们之前曾描述过72 kDa和74 kDa的肽结合蛋白(PBP72/74),它们被认为在抗原加工过程中发挥作用,并且在血清学上与70 kDa热休克蛋白(hsp70)家族相关。在此,我们报告了通过使用从纯化蛋白获得的氨基酸序列信息完成的小鼠和人类中编码PBP74的cDNA的克隆和测序。我们表明,PBP74与hsp70家族成员高度同源,但重要的是,它与该家族的任何已知成员都不相同。对cDNA核苷酸序列的检查表明,它编码一个46个残基的N端肽,该肽不存在于成熟蛋白中。PBP74 cDNA的体外转录和翻译证实,它编码一种比成熟蛋白更大的PBP74形式。前序列不符合已知的细胞器靶向序列基序,目前其功能尚不清楚。通过共聚焦显微镜,使用针对PBP74 N端16个残基的特异性抗体,PBP74定位于细胞质小泡,而不是细胞核、线粒体或质膜。通过RNA滤膜杂交分析,在所有测试的细胞类型中都检测到了PBP74 mRNA。与应激诱导的hsp70 mRNA显著增加不同,细胞暴露于热休克不会导致PBP74 mRNA水平增加。因此,PBP74似乎是hsp70家族的一个组成型新成员。