Azen E, Lyons K M, McGonigal T, Barrett N L, Clements L S, Maeda N, Vanin E F, Carlson D M, Smithies O
Proc Natl Acad Sci U S A. 1984 Sep;81(17):5561-5. doi: 10.1073/pnas.81.17.5561.
The salivary protein gene complex consists of a series of loci coding for related but distinct proline-rich proteins (PRPs) found chiefly in saliva. We have screened a library of human genomic DNA fragments in bacteriophage lambda Charon 4A with a PRP cDNA synthesized and cloned from rat parotid gland mRNA. Two phages (PRP1 and PRP2) hybridizing to the rat probe under moderately stringent conditions contain related but not identical DNAs. Preliminary nucleotide sequence data indicate that both DNAs include regions comprised of nearly identical tandemly repeated sequences, each able to code for about 21 amino acids. The decoded consensus repeat sequence is homologous to the repeating amino acid units found by others in human PRPs. This and other features demonstrate that these two clones are members of the PRP gene family. Polymorphic differences between the DNAs of different individuals were observed after probing digests of human genomic DNA with a HinfI fragment from PRP1. These DNA polymorphisms reflect size differences, possibly caused by frequent unequal crossing-over between the repeated units in the PRP genes.
唾液蛋白基因复合体由一系列基因座组成,这些基因座编码主要存在于唾液中的相关但不同的富含脯氨酸的蛋白质(PRP)。我们用从大鼠腮腺mRNA合成并克隆的PRP cDNA筛选了噬菌体λCharon 4A中的人类基因组DNA片段文库。在中等严格条件下与大鼠探针杂交的两个噬菌体(PRP1和PRP2)含有相关但不相同的DNA。初步核苷酸序列数据表明,两个DNA都包含由几乎相同的串联重复序列组成的区域,每个区域能够编码约21个氨基酸。解码的共有重复序列与其他人在人类PRP中发现的重复氨基酸单元同源。这一特征和其他特征表明这两个克隆是PRP基因家族的成员。用PRP1的HinfI片段探测人类基因组DNA消化物后,观察到不同个体DNA之间的多态性差异。这些DNA多态性反映了大小差异,可能是由PRP基因中重复单元之间频繁的不等交换引起的。