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Vol. 13, Issue 12, 4256-4265, December 2002

Department of Biological Chemistry, Weizmann Institute of Science,
Rehovot 76100, Israel
The 260-kDa heterodimeric Gal/GalNAc-specific Lectin (Gal-lectin)
of Entamoeba histolytica dissociates under reducing
conditions into a heavy (hgl, 170 kDa) and a light subunit (lgl,
35 kDa). We have previously shown that inhibition of expression of the 35-kDa subunit by antisense RNA causes a decrease in virulence. To
further understand the role of the light subunit of the Gal-lectin in
pathogenesis, amoebae were transfected with plasmids encoding intact,
mutated, and truncated forms of the light subunit lgl1 gene. A transfectant in which the 55 N-terminal amino acids of the lgl
were removed, overproduced an N-truncated lgl protein (32 kDa), which
replaced most of the native 35-kDa lgl in the formation of the
Gal-lectin heterodimeric complex and exerted a dominant negative
effect. Amoebae transfected with this construct showed a significant
decrease in their ability to adhere to and kill mammalian cells as well
as in their capacity to form rosettes with and to phagocytose
erythrocytes. In addition, immunofluorescence confocal microscopy of
this transfectant with anti-Gal-lectin antibodies showed an impaired
ability to cap. These results indicate that the light subunit has a
role in enabling the clustering of Gal-lectin complexes and that its
N-truncation affects this function, which is required for virulence.
Corresponding author. E-mail address:
david.mirelman{at}weizmann.ac.il.
*
Present address: Department of Molecular Microbiology, The Bruce
Rappaport Faculty of Medicine, Technion, POB 9649, Haifa 31096, Israel.
Tamara Stolarsky died on September 27, 2001.
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