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Differential expression of four human dynamin-like protein variants in brain tumors

  • Chang Han Chen
  • , Shen Long Howng
  • , Shiuh Lin Hwang
  • , Chen Kung Chou
  • , Chen Hua Liao
  • , Yi Ren Hong*
  • *Corresponding author for this work
  • Kaohsiung Medical University
  • Veterans General Hospital-Taipei

Research output: Contribution to journal › Journal Article › peer-review

15 Scopus citations

Abstract

Dynamin-like protein, a large GTP-binding protein, has recently been cloned, and studies have suggested that it is involved in the formation of coated vesicles. In this report, the differential expression of four human dynamin-like protein splice variants (HdynIV-wildtype [WT], -11, -26, and - 37) from various brain tumors was identified by reverse transcription/polymerase chain reaction (RT-PCR). One novel variant (HdynIV- 11), not described previously, was identified. The four alternatively spliced variants exhibited tissue specificity in normal tissues. The HdynIV-WT was strongly expressed in the brain, whereas HdynIV-37 was expressed in all tissues examined. Moreover, HdynIV-26 was dominant in the liver and apparently overexpressed in all astrocytomas and most meningiomas and adenomas. This report suggests that HdynIV-26 may cause aberrant protein trafficking and alter vesicle formation in brain tumors. Our results also suggest that dynamin-like protein is associated with various brain tumors and, more importantly, that aberrant expression of the HdynIV-26 variant may play a role in brain tumorigenesis.

Original languageEnglish
Pages (from-to)189-194
Number of pages6
JournalDNA and Cell Biology
Volume19
Issue number3
DOIs
StatePublished - 2000
Externally publishedYes

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

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