Cloning of cDNA coding for connective tissue activating peptide III from a human platelet-derived lambda gt11 expression library.

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Citation

Wenger RH, Wicki AN, Walz A, Kieffer N, Clemetson KJ

Cloning of cDNA coding for connective tissue activating peptide III from a human platelet-derived lambda gt11 expression library.

Blood. 1989 May 1;73(6):1498-503.

PubMed ID
2713489 [ View in PubMed
]
Abstract

We report here the cloning of the cDNA coding for platelet connective tissue-activating peptide-III (CTAP-III) from a lambda gt11 expression library prepared using messenger RNA (mRNA) isolated from human platelets. The open reading frame of the clone coded for a protein with 128 amino acid residues. Since the precursor of CTAP-III, platelet basic protein (PBP is 94 amino acids long, the 5'-translated region of the cDNA codes for a leader sequence 34 amino acids long. This leader sequence, like the sequence of mature CTAP-III, shows significant homology to the sequence of platelet factor 4 (PF4), the only other platelet specific alpha-granule protein cloned until now, from a human erythroleukemic (HEL) cell line-derived cDNA library. These leader sequences are probably critical for targeting such proteins to the alpha-granule. Northern blot hybridization with platelet and megakaryocyte mRNA shows a single species mRNA of approximately 0.8 kb, suggesting that the corresponding cDNA is full length. The cloning of platelet specific CTAP-III provides additional evidence for the platelet specificity of the cDNA library used.

DrugBank Data that Cites this Article

Polypeptides
NameUniProt ID
Platelet basic proteinP02775Details