Review Article

Susceptibility to Dental Caries and the Salivary Proline-Rich Proteins

Table 4

Basic PRP genes and products1.

LocusName of encoded protein2PartialResidues3

PRB1:Basic salivary proline-rich protein 1 1–392
Pe (II-2) 17–91
Ps2 92–392
IB-9 (PmF) 91–152
Ps1 (deletion)4 92–153; 213–392
Con2 (deletion)4152–194; 214–274
IB-6 (PmS, P-I)5275–392

PRB2:Basic salivary proline-rich protein 2 1–416
(Con1 glycoprotein)IB-1 17–112
IB-7 (P-G)113–1716 or 1747
Con1175–299
IB-8C (P-F)299–359
IB-4 (P-H)361–416

PRB3:Basic salivary proline-rich protein 31–309
(Parotid salivary glycoprotein G1)G117–309

PRB4:Basic salivary proline-rich protein 4 1–310
(Parotid o protein)Protein N1 17–39
(Salivary proline-rich protein II-1)Glycosylated Pr A 40–177
IB-5 (P-D)241–310

1From Azen et al. [70, Table 1] and from Ayad et al. [31, Table 3] updated from the Protein Knowledgebase website (UniProt.org) which was accessed from GeneCards or Epasy websites.
2There is extensive polymorphism (see text). Many proteins encoded by PRB1 and PRB2 [60], Ps1, Ps2, PmS PmF, Pe, Con2 are not included in the Protein Knowledgebase, or (for Con1) the composition is improperly indicated as an alternative name for the whole gene product, which it is not (see Figure 5).
3First set of numbers for each gene indicates the full length encoded polypeptide of each gene. The numbers beneath indicate the fragments of the polypeptide that are commonly found in parotid saliva secretions. The N-terminal 16 amino acids comprise a secretion signal which is removed prior to secretion (Figure 4).
4Deletion of repeating sequences 154–212 or 195–213
5Sequence is identical to IB-8c plus IB-4. IB-4 (P-H) is not normally released from IB-6 because residues 333–336 are QSAR (Figure 4). IB-4 (P-H) is normally derived from PRB2 where the last 4 C-terminal amino acids of IB-8c (356–360) are RSAR (see text, Section 6). At this time, Uniprot.org appears to have incorrectly listed P-H as produced by PRB1, but IB4 correctly from PRB2. P-H is an alternative name for IB4 and would only be produced from PRB1 if the codon for Q (residue 333) is mutated to R, an uncommon A to G mutation, or an even less common double mutation.
6,7Termination codon in PRB2S, or cleavage in PRB2M (see legend to Figure 5).