Schwartz E, Shen D, Aebersold R, McGrath J M, Pichersky E, Green B R
Biology Department, University of Michigan, Ann Arbor 48109.
FEBS Lett. 1991 Mar 25;280(2):229-34. doi: 10.1016/0014-5793(91)80299-i.
Tryptic peptide sequences from the 22 kDa polypeptide of tomato LHCI were used to construct a probe for gene cloning. The two genes cloned, cab11 and cab12, encode proteins of 251 and 250 residues that are 88% identical in overall amino acid sequence and 93% identical in the deduced mature protein. Each gene is present in a single copy per haploid genome; cab11 on chromosome 3 and cab12 on chromosome 6, and each has 2 introns located in similar positions to introns in other members of the Chl a/b-binding (CAB) protein gene family. Comparison of the amino acid sequences of LHCI, LHCII, CP29 and CP24 polypeptides confirms that all CABs share two regions of very high similarity which include the first and third transmembrane helices and the stroma-exposed sequences preceding them. However, near the N-terminus and between the conserved regions, the LHCI polypeptides have sequence motifs which appear to be PSI-specific.
来自番茄光系统I捕光复合体(LHCI)22 kDa多肽的胰蛋白酶肽序列被用于构建基因克隆探针。克隆出的两个基因cab11和cab12,编码的蛋白质分别有251和250个残基,其整体氨基酸序列的一致性为88%,推导的成熟蛋白的一致性为93%。每个基因在单倍体基因组中以单拷贝形式存在;cab11位于3号染色体上,cab12位于6号染色体上,且每个基因都有2个内含子,其位置与叶绿素a/b结合(CAB)蛋白基因家族其他成员中的内含子位置相似。对LHCI、LHCII、CP29和CP24多肽的氨基酸序列进行比较证实,所有CAB蛋白都有两个高度相似的区域,包括第一个和第三个跨膜螺旋以及它们之前暴露于基质的序列。然而,在靠近N端以及保守区域之间,LHCI多肽具有似乎是光系统I特异性的序列基序。