Evidence map›Paper›PMID 31377908›Full record

ArticleParasitology research2019

Identification of a new type of haematopoietic progenitor kinase-interacting protein (HIP-55) in Aedes aegypti mosquito haemocytes and its involvement in immunity-like functions in mosquito: a molecular study.

M Mohiadeen Batcha, A Sajith Ahamed, Chiung Fang Peng

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Article in Parasitology research, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
0.1field-weighted citation impact, top 54% of its field
1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

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0 citing papers in PubMed, 2 citations in OpenAlex.

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4 · The record

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5 · Who and what money

Authors and funding

3 authors at 2 institutions in 2 countries.

M Mohiadeen BatchaDepartment of Zoology, HKRH College, Uthamapalayam, Theni District, Tamil Nadu, India. mbatcha73@gmail.com.ORCID http://orcid.org/0000-0001-8610-9020
A Sajith AhamedDepartment of Microbiology, HKRH College, Uthamapalayam, Theni District, Tamil Nadu, India.
Chiung Fang PengFuga Biotechnology, Chongqing S. Rd, Zhongzheng Dist, Taipei - 100, Taiwan.
National Yang Ming Chiao Tung University · TWTaiGen Biotechnology (Taiwan) · TW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In this study, we characterize the HIP-55 protein in the mosquito Aedes aegypti for the first time. HIP-55 is a 55-kDa HPK1-interacting protein that is also called SH3P7. HIP-55 constitutively binds HPK1 'via' an HPK1 proline-rich motif 2(PR2) through its C-terminal SH3 domain. HIP-55 critically interacts with ZAP-70, and this interaction was induced by TCR signalling. ZAP-70 phosphorylated HIP-55 at Tyr-334 and Tyr-344 in vitro and in vivo. In our previous findings, AaZAP gene expression strongly proved that AaZAP-70 was involved in immunity-like functions in mosquito. Northern blot analysis of HIP-55 mRNA expression confirmed that it is only expressed in the abdomen and haemocyte tissues; this prediction correlates 100% and a polyclonal antibody also confirmed its localization in haemocytes and the abdomen. We prepared extracts to show the cytoplasmic expression (CE) of this protein. Previous results had proven that this protein is secreted from the cytoplasm; thus, we confirmed here that the protein is a cytoplasmic adaptor protein in mosquitoes and mammalian systems. Furthermore, our polyclonal antibody against HIP-55 also demonstrated that this protein is found in haemocytes and abdomen tissues, which assumes that the protein may be involved in phagocytic-like functions. RNAi (siRNA) silencing studies were used to degrade mosquito HIP-55; however, silencing only slightly affected the HIP-55 sequence and the gene transcriptional level. To characterize this protein, we cloned 609 bp from the 1.6-kb full-length cDNA using a pET28 vector for polyclonal antibody production. Graphical abstract.

Indexed as

AedesAnimalsHemocytesMicrofilament ProteinsPhosphorylationProtein BindingProtein Serine-Threonine KinasesRNA InterferenceRNA, MessengerRNA, Small InterferingSignal Transductionsrc Homology DomainsZAP-70 Protein-Tyrosine KinaseMicrofilament ProteinsProtein Serine-Threonine KinasesRNA, MessengerRNA, Small InterferingZAP-70 Protein-Tyrosine KinaseAedes aegyptiAn actin-binding adaptor proteinHaemocytesHIP-55HPK1SH3 domainZAP-70

Identifiers

PMID31377908
OpenAlexW2964659544

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.