Sequence of a putative human housekeeping gene (HK33) localized on chromosome 1
- PMID: 8076834
- DOI: 10.1016/0378-1119(94)90308-5
Sequence of a putative human housekeeping gene (HK33) localized on chromosome 1
Abstract
A gene (HK33) localized on human chromosome 1 has been detected by crossreaction of its fusion protein with a monospecific antiserum directed against human vitamin-D-binding protein (hDBP; group-specific component). Its cDNA sequence analysis showed no evident homologies neither to the sequence encoding hDBP nor to any other sequence. The largest cDNA clone of 3.2 kb includes a 897-bp coding region and a large 3' untranslated region with at least four polyadenylation sites. Further cDNA amplification using PCR demonstrated a total cDNA length of approx. 3.7 kb. Northern blot analysis revealed signals at about 2.2-2.5 kb and 4.0 kb, the shorter transcripts representing mRNAs using one of the two polyadenylation sites at about 2.0 kb. Synthesis of the 299-amino-acid polypeptide (33 kDa) in the bacterial host, with subsequent Western blot analysis, verified the sequence-specific recognition by the hDBP-specific antiserum. The search of protein databanks revealed no homology of HK33 to any known sequence. Since the gene is transcribed in all cells and tissues tested so far, it is a strong candidate for another housekeeping gene.
Similar articles
-
[cDNA cloning, subcellular localization and tissue expression of a new human Krüppel-like transcription factor: human basic Krüppel-like factor (hBKLF)].Yi Chuan Xue Bao. 2003 Jan;30(1):1-9. Yi Chuan Xue Bao. 2003. PMID: 12812068 Chinese.
-
Complex RNA processing of TDRKH, a novel gene encoding the putative RNA-binding tudor and KH domains.Gene. 2000 Apr 4;246(1-2):209-18. doi: 10.1016/s0378-1119(00)00087-1. Gene. 2000. PMID: 10767542
-
Molecular cloning and characterization of a human cDNA and gene encoding a novel acid ceramidase-like protein.Genomics. 1999 Dec 1;62(2):232-41. doi: 10.1006/geno.1999.5953. Genomics. 1999. PMID: 10610717
-
The novel human HUEL (C4orf1) gene maps to chromosome 4p12-p13 and encodes a nuclear protein containing the nuclear receptor interaction motif.Genomics. 1999 Jul 15;59(2):224-33. doi: 10.1006/geno.1999.5856. Genomics. 1999. PMID: 10409434
-
The human decorin gene: intron-exon organization, discovery of two alternatively spliced exons in the 5' untranslated region, and mapping of the gene to chromosome 12q23.Genomics. 1993 Jan;15(1):146-60. doi: 10.1006/geno.1993.1022. Genomics. 1993. PMID: 8432526
Cited by
-
PEX13 is mutated in complementation group 13 of the peroxisome-biogenesis disorders.Am J Hum Genet. 1999 Sep;65(3):621-34. doi: 10.1086/302534. Am J Hum Genet. 1999. PMID: 10441568 Free PMC article.
-
Pex19p interacts with Pex3p and Pex10p and is essential for peroxisome biogenesis in Pichia pastoris.Mol Biol Cell. 1999 Jun;10(6):1745-61. doi: 10.1091/mbc.10.6.1745. Mol Biol Cell. 1999. PMID: 10359594 Free PMC article.
-
Farnesylation of pex19p is required for its structural integrity and function in peroxisome biogenesis.J Biol Chem. 2009 Jul 31;284(31):20885-96. doi: 10.1074/jbc.M109.016584. Epub 2009 May 18. J Biol Chem. 2009. PMID: 19451657 Free PMC article.
-
Pex19p, a farnesylated protein essential for peroxisome biogenesis.Mol Cell Biol. 1998 Jan;18(1):616-28. doi: 10.1128/MCB.18.1.616. Mol Cell Biol. 1998. PMID: 9418908 Free PMC article.
-
Human PEX19: cDNA cloning by functional complementation, mutation analysis in a patient with Zellweger syndrome, and potential role in peroxisomal membrane assembly.Proc Natl Acad Sci U S A. 1999 Mar 2;96(5):2116-21. doi: 10.1073/pnas.96.5.2116. Proc Natl Acad Sci U S A. 1999. PMID: 10051604 Free PMC article.
Publication types
MeSH terms
Substances
Associated data
- Actions
LinkOut - more resources
Full Text Sources
Medical
Molecular Biology Databases