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可变剪接产生了长须罗蛉几丁质酶不同的结构域结构组织。

Alternative splicing originates different domain structure organization of Lutzomyia longipalpis chitinases.

作者信息

Ortigão-Farias João Ramalho, Di-Blasi Tatiana, Telleria Erich Loza, Andorinho Ana Carolina, Lemos-Silva Thais, Ramalho-Ortigão Marcelo, Tempone Antônio Jorge, Traub-Csekö Yara Maria

机构信息

Laboratório de Biologia Molecular de Parasitos e Vetores, Instituto Oswaldo Cruz, Fundação Oswaldo Cruz-Fiocruz, Rio de Janeiro, RJ, Brasil.

出版信息

Mem Inst Oswaldo Cruz. 2018 Feb;113(2):96-101. doi: 10.1590/0074-02760170179.

Abstract

BACKGROUND The insect chitinase gene family is composed by more than 10 paralogs, which can codify proteins with different domain structures. In Lutzomyia longipalpis, the main vector of visceral leishmaniasis in Brazil, a chitinase cDNA from adult female insects was previously characterized. The predicted protein contains one catalytic domain and one chitin-binding domain (CBD). The expression of this gene coincided with the end of blood digestion indicating a putative role in peritrophic matrix degradation. OBJECTIVES To determine the occurrence of alternative splicing in chitinases of L. longipalpis. METHODS We sequenced the LlChit1 gene from a genomic clone and the three spliced forms obtained by reverse transcription polymerase chain reaction (RT-PCR) using larvae cDNA. FINDINGS We showed that LlChit1 from L. longipalpis immature forms undergoes alternative splicing. The spliced form corresponding to the adult cDNA was named LlChit1A and the two larvae specific transcripts were named LlChit1B and LlChit1C. The B and C forms possess stop codons interrupting the translation of the CBD. The A form is present in adult females post blood meal, L4 larvae and pre-pupae, while the other two forms are present only in L4 larvae and disappear just before pupation. Two bands of the expected size were identified by Western blot only in L4 larvae. MAIN CONCLUSIONS We show for the first time alternative splicing generating chitinases with different domain structures increasing our understanding on the finely regulated digestion physiology and shedding light on a potential target for controlling L. longipalpis larval development.

摘要

背景 昆虫几丁质酶基因家族由10多个旁系同源基因组成,这些基因可编码具有不同结构域结构的蛋白质。在巴西内脏利什曼病的主要传播媒介长须罗蛉中,先前已对成年雌性昆虫的一种几丁质酶cDNA进行了表征。预测的蛋白质包含一个催化结构域和一个几丁质结合结构域(CBD)。该基因的表达与血液消化结束同时发生,表明其在围食膜降解中可能发挥作用。目的 确定长须罗蛉几丁质酶中可变剪接的发生情况。方法 我们对来自基因组克隆的LlChit1基因以及使用幼虫cDNA通过逆转录聚合酶链反应(RT-PCR)获得的三种剪接形式进行了测序。研究结果 我们发现长须罗蛉未成熟形式的LlChit1会发生可变剪接。与成年cDNA对应的剪接形式命名为LlChit1A,两种幼虫特异性转录本命名为LlChit1B和LlChit1C。B和C形式具有终止密码子,会中断CBD的翻译。A形式存在于成年雌性血餐后、L4幼虫和预蛹中,而其他两种形式仅存在于L4幼虫中,并在化蛹前消失。通过蛋白质免疫印迹仅在L4幼虫中鉴定出两条预期大小的条带。主要结论 我们首次展示了可变剪接产生具有不同结构域结构的几丁质酶,这增加了我们对精细调节的消化生理学的理解,并为控制长须罗蛉幼虫发育的潜在靶点提供了线索。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6c45/5722264/33e83bd56626/0074-0276-mioc-113-02-0096-gf01.jpg

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