Miller P W, Dunn W I, Schmidt R R
Department of Microbiology and Cell Science, University of Florida, Gainesville 32611, USA.
Plant Mol Biol. 1998 May;37(2):243-63. doi: 10.1023/a:1005921018137.
Chlorella sorokiniana has seven ammonium-inducible, chloroplastic NADP-specific glutamate dehydrogenase (NADP-GDH) isozymes composed of varying ratios of alpha- and beta-subunits. Southern blot and allele-specific PCR analyses indicate that the C. sorokiniana genome possesses a single 7178 bp nuclear NADP-GDH gene. cDNA cloning and sequencing, 5'-RACE-PCR analysis, and RNase protection analysis identified two NADP-GDH mRNAs that are identical with the exception of a 42 nt sequence located within the 5'-coding region of the longer mRNA. The 42 nt sequence, termed an auxon because it serves as an exon or intron, appears to undergo alternative splicing from the precursor mRNA by a process that is regulated by both nutritional and environmental signals. Depending upon whether the auxon is included or excluded in a mature mRNA, the gene can be considered to consist of 22 or 23 exons, respectively. The 2074 and 2116 nt mRNAs encode precursor proteins of 56,350 and 57,850 Da, respectively. The N-termini of the purified mature alpha- and beta-subunits were sequenced, identifying full-length subunits of 53,501 and 52,342 Da, respectively. The sequences of the subunits are identical except for an 11 amino acid extension at the N-terminus of the alpha-subunit. The alpha-subunit has an additional alpha-helical domain at its N-terminus compared with the beta-subunit. By correlating the abundances of the two mRNAs with the levels (and relative turnover rates) of the alpha- and beta-subunit antigens during induction in Chlorella, the larger mRNA is proposed to encode the larger subunit.
索氏小球藻有七种铵诱导型、叶绿体NADP特异性谷氨酸脱氢酶(NADP-GDH)同工酶,由不同比例的α亚基和β亚基组成。Southern杂交和等位基因特异性PCR分析表明,索氏小球藻基因组拥有一个单一的7178 bp核NADP-GDH基因。cDNA克隆与测序、5'-RACE-PCR分析以及核糖核酸酶保护分析鉴定出两种NADP-GDH mRNA,它们除了在较长mRNA的5'-编码区内有一个42 nt的序列外完全相同。这个42 nt的序列被称为辅助元件,因为它既可以作为外显子也可以作为内含子,似乎通过一个受营养和环境信号调控的过程从前体mRNA进行可变剪接。根据辅助元件是否包含在成熟mRNA中,该基因可分别被认为由22个或23个外显子组成。2074 nt和2116 nt的mRNA分别编码56,350 Da和57,850 Da的前体蛋白。对纯化的成熟α亚基和β亚基的N末端进行了测序,分别鉴定出全长为53,501 Da和52,342 Da的亚基。除了α亚基N末端有一个11个氨基酸的延伸外,两个亚基的序列相同。与β亚基相比,α亚基在其N末端有一个额外的α螺旋结构域。通过将两种mRNA的丰度与小球藻诱导过程中α亚基和β亚基抗原的水平(以及相对周转率)进行关联,推测较大的mRNA编码较大的亚基。