Mazumdar-Leighton S, Broadway R M
Department of Entomology, Cornell University, New York State Agricultural Experiment Station, Geneva, NY 14456, USA.
Insect Biochem Mol Biol. 2001 Apr 27;31(6-7):645-57. doi: 10.1016/s0965-1748(00)00169-7.
Midgut trypsins insensitive to inhibition by the soybean trypsin inhibitor (STI) were found to be transcriptionally regulated in A. ipsilon and H. zea larvae feeding on STI, as demonstrated by injections with actinomycin, a transcriptional inhibitor, which abolished the production of these STI-insensitive trypsins. The induced, STI-insensitive trypsins differed from the constitutive, STI-sensitive trypsins in their susceptibility to inhibitors based on sizes, suggesting that the induced enzymes limited access to their active site by blocking bulky inhibitors. Twenty midgut cDNA fragments(1) were amplified using trypsin-specific PCR primers and at least twelve were shown to encode structurally diverse trypsins. High sequence diversity was observed for both the enzymes encoded by STI-induced mRNAs and those from larvae that had not been exposed to STI. Northern blots showed that midgut mRNAs hybridizing to various trypsin cDNA probes were either transcribed de novo or up-regulated following ingestion of STI. Southern hybridizations indicated the presence of multiple trypsin gene families in the insect genomes. The complete sequence of a trypsin gene(1) from A. ipsilon (AiT9) revealed the presence of three introns. Comparison of 5' upstream sequences(1) from AiT9 and AiT6 genes from A. ipsilon revealed putative TATA box and disparate regulatory motifs, within 500 bp of each translational start site.
在以大豆胰蛋白酶抑制剂(STI)为食的黑地老虎和玉米螟幼虫中,发现对STI抑制不敏感的中肠胰蛋白酶受到转录调控。用转录抑制剂放线菌素注射证明了这一点,放线菌素消除了这些对STI不敏感的胰蛋白酶的产生。诱导产生的、对STI不敏感的胰蛋白酶与组成型的、对STI敏感的胰蛋白酶在对基于大小的抑制剂的敏感性方面有所不同,这表明诱导产生的酶通过阻断大分子抑制剂来限制其活性位点的可及性。使用胰蛋白酶特异性PCR引物扩增了20个中肠cDNA片段,其中至少12个被证明编码结构多样的胰蛋白酶。对由STI诱导的mRNA编码的酶和未接触过STI的幼虫的酶都观察到了高度的序列多样性。Northern印迹显示,与各种胰蛋白酶cDNA探针杂交的中肠mRNA要么是从头转录的,要么在摄入STI后上调。Southern杂交表明昆虫基因组中存在多个胰蛋白酶基因家族。黑地老虎一个胰蛋白酶基因(AiT9)的完整序列显示存在三个内含子。对黑地老虎AiT9和AiT6基因5'上游序列的比较揭示了在每个翻译起始位点500 bp内存在推定的TATA盒和不同的调控基序。