๐ Homozygous L-SIGN (CLEC4M) plays a protective role in SARS coronavirus infection
Severe acute respiratory syndrome (SARS) is caused by infection of a previously undescribed coronavirus (CoV). L-SIGN, encoded by CLEC4M (also known as CD209L), is a SARS-CoV binding receptor that has polymorphism in its extracellular neck region encoded by the tandem repeat domain in exon 4. Our genetic risk association study shows that individuals homozygous for CLEC4M tandem repeats are less susceptible to SARS infection. L-SIGN is expressed in both non-SARS and SARS-CoV-infected lung. Compared with cells heterozygous for L-SIGN, cells homozygous for L-SIGN show higher binding capacity for SARS-CoV, higher proteasome-dependent viral degradation and a lower capacity for trans infection. Thus, homozygosity for L-SIGN plays a protective role during SARS infection. ยฉ 2006 Nature Publishing Group.
author
๐ค Chan, Vera S.F.
๐ค Chan, Kelvin Y.K.
๐ค Chen, Yongxiong
๐ค Poon, Leo L.M.
๐ค Cheung, Annie N.Y.
๐ค Zheng, Bojian
๐ค Chan, Kwok Hung
๐ค Mak, William
๐ค Ngan, Hextan Y.S.
๐ค Xu, Xiaoning
๐ค Screaton, Gavin
๐ค Tam, Paul K.H.
๐ค Austyn, Jonathan M.
๐ค Chan, Li Chong
๐ค Yip, Shea Ping
๐ค Peiris, Malik
๐ค Khoo, Ui Soon
๐ค Lin, Chen Lung S.
year
โฐ 2006
journal
๐ Nature Genetics
issn
๐ 10614036 15461718
volume
38
number
1
page
38-46
citedbycount
81
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