Human augmenter of liver regeneration: molecular cloning, biological activity and roles in liver regeneration
The complete amino acid sequence of human augmenter of liver regeneration (hALR) was reported by deduction from nucleotide sequence of its complementary DNA . The cDNA for hALR was isolated by screening a human fetal liver cDNA library and the sequencing of this insert revealed an open reading frame...
Saved in:
Published in: | Science China. Life sciences Vol. 40; no. 6; pp. 642 - 647 |
---|---|
Main Author: | |
Format: | Journal Article |
Language: | English |
Published: |
China
Springer Nature B.V
01-12-1997
|
Subjects: | |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Summary: | The complete amino acid sequence of human augmenter of liver regeneration (hALR) was reported by deduction from nucleotide sequence of its complementary DNA . The cDNA for hALR was isolated by screening a human fetal liver cDNA library and the sequencing of this insert revealed an open reading frame encoding a protein with 125aa and highly homologous (87% ) with rat ALR encoding sequence. The recombinant hALR expressed from its cDNA in transient expression experiments in cos-7 cells could stimulate DNA synthesis of HTC hepatoma cell in the dose-dependent and heat-resistant way. Northern blot analysis with rat ALR cDNA as probe confirmed that ALR mRNA was expressed in the normal rat liver at low level and that dramatically increased in the regenerating liver after partial hepatectomied rat. This size of hALR mRNA is 1.4 kb long and expressed in human fetal liver, kidney and testis. These findings indicated that liver itself may be the resource of ALR and suggested that ALR seems to be an im-portant parac |
---|---|
Bibliography: | YANG Xiaoming, XIE Ling, QIU ZhaohuaWU Zuze HE Fuchu(Department of Experimental Hematology, Beijing Institute of Radiation Medicine, Beijing 100850, China) 11-5841/Q ObjectType-Article-2 SourceType-Scholarly Journals-1 ObjectType-Feature-1 content type line 23 ObjectType-Article-1 ObjectType-Feature-2 |
ISSN: | 1674-7305 1006-9305 1869-1889 1862-2798 |
DOI: | 10.1007/BF02882695 |