Isolation and characterization of cDNA clones encoding pig gastric mucin.
Isolation and characterization of cDNA clones encoding pig gastric mucin.
复制标题
编码猪胃粘蛋白的 cDNA 克隆的分离和表征。
DOI:
10.1042/bj3080089
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发表时间:
1995
期刊:
影响因子:
--
通讯作者:
LaMont,JT
中科院分区:
文献类型:
--
作者:
Turner,BS;Bhaskar,KR;Hadzopoulou-Cladaras,M;Specian,RD;LaMont,JT
Polyclonal antibodies raised to deglycosylated pig gastric mucin were used to screen a cDNA library constructed with pig stomach mucosal mRNA. Immunocytochemistry indicated that the antibody recognizes intracellular and secreted mucin in surface mucous cells of pig gastric epithelium. A total of 70 clones producing proteins immunoreactive to this antibody were identified, two of which (PGM-2A,9B) were fully sequenced from both ends. Clone PGM-9B hybridized to a polydisperse mRNA (3-9 kb) from pig stomach, but not liver, intestine or spleen, nor to mRNA from human, mouse, rabbit or rat stomach. Sequence analysis indicated that PGM-9B encodes 33 tandem repeats of a 16-amino-acid consensus sequence rich in serine (46%) and threonine (17%). Using the restriction enzyme MwoI, which has a single target site in the repeat, it was demonstrated that PGM-9B consists entirely of this tandem repeat. Southern-blot analysis indicated that the repeat region is contained in a 20 kb HindIII-EcoRI fragment, and BamHI digestion suggested that most of the repeats are contained in a 10 kb fragment. In situ hybridization with an antisense probe to PGM-9B showed an intense signal in the entire gastric gland. Clone PGM-2A also contains the same repeat sequence as 9B, but, in addition, has a 64-amino-acid-long non-repeat region at its 5′ end. Interestingly the non-repeat region of PGM-2A has five cysteine residues, the arrangement of which is identical with that reported for human intestinal mucin gene MUC2.
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DOI:
10.1152/ajprenal.1978.235.4.f367
发表时间:
1978
期刊:
The American journal of physiology
影响因子:
--
作者:
G. Shareghi;L. Stoner
通讯作者:
L. Stoner
影响因子:
2.4
作者:
J. Krieger
通讯作者:
J. Krieger
影响因子:
1.5
作者:
E. Horowitz;J. Schmidt
通讯作者:
J. Schmidt
影响因子:
--
作者:
P. Armon
通讯作者:
P. Armon
DOI:
--
发表时间:
1983
期刊:
The Lancet
影响因子:
--
作者:
M. Gregory;M. Mansell
通讯作者:
M. Mansell