Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
3
pubmed:dateCreated
1984-7-19
pubmed:abstractText
Multiple sulfatase deficiency (MSD) is an inherited disorder characterized by deficient activity of seven different sulfatases. Genetic complementation for steroid sulfatase (STS), arylsulfatase A, and N-acetylgalactosamine 6-SO4 sulfatase was demonstrated in somatic cell hybrids between MSD fibroblasts and mouse cells ( LA9 ) or Chinese hamster cells ( CHW ). In an electrophoretic system that separates human and rodent STS isozymes, enzyme from hybrids migrated as human enzyme. We concluded that the rodent cell complemented the MSD deficiency and allowed normal expression of the STS structural gene. Some MSD- LA9 hybrids showed significant levels of human arylsulfatase A activity, as shown by the immunoprecipitation of active enzyme by human-specific antiserum. Complementation was also suggested for N-acetylgalactosamine 6- sulfatate sulfatase (GalNAc-6S sulfatase) in several MSD- LA9 hybrids by the demonstration of a significant increase in activity (10-fold) over that of the GalNAc-6S sulfatase-deficient parental mouse and MSD cells. Thus, it was possible to demonstrate complementation for more than one sulfatase in a single MSD-rodent hybrid. Normal levels of sulfatase activity in hybrids indicate that the sulfatase structural genes are intact in MSD cells.
pubmed:grant
pubmed:commentsCorrections
http://linkedlifedata.com/resource/pubmed/commentcorrection/6731437-1028164, http://linkedlifedata.com/resource/pubmed/commentcorrection/6731437-1127527, http://linkedlifedata.com/resource/pubmed/commentcorrection/6731437-116130, http://linkedlifedata.com/resource/pubmed/commentcorrection/6731437-118467, http://linkedlifedata.com/resource/pubmed/commentcorrection/6731437-120190, http://linkedlifedata.com/resource/pubmed/commentcorrection/6731437-1203481, http://linkedlifedata.com/resource/pubmed/commentcorrection/6731437-120987, http://linkedlifedata.com/resource/pubmed/commentcorrection/6731437-13663253, http://linkedlifedata.com/resource/pubmed/commentcorrection/6731437-25410, http://linkedlifedata.com/resource/pubmed/commentcorrection/6731437-26836, http://linkedlifedata.com/resource/pubmed/commentcorrection/6731437-27985, http://linkedlifedata.com/resource/pubmed/commentcorrection/6731437-293682, http://linkedlifedata.com/resource/pubmed/commentcorrection/6731437-4265903, http://linkedlifedata.com/resource/pubmed/commentcorrection/6731437-4272659, http://linkedlifedata.com/resource/pubmed/commentcorrection/6731437-4850305, http://linkedlifedata.com/resource/pubmed/commentcorrection/6731437-523191, http://linkedlifedata.com/resource/pubmed/commentcorrection/6731437-6108562, http://linkedlifedata.com/resource/pubmed/commentcorrection/6731437-6119929, http://linkedlifedata.com/resource/pubmed/commentcorrection/6731437-6122572, http://linkedlifedata.com/resource/pubmed/commentcorrection/6731437-6793566, http://linkedlifedata.com/resource/pubmed/commentcorrection/6731437-6812049, http://linkedlifedata.com/resource/pubmed/commentcorrection/6731437-6935682, http://linkedlifedata.com/resource/pubmed/commentcorrection/6731437-694728, http://linkedlifedata.com/resource/pubmed/commentcorrection/6731437-7333023, http://linkedlifedata.com/resource/pubmed/commentcorrection/6731437-7394700, http://linkedlifedata.com/resource/pubmed/commentcorrection/6731437-7458940, http://linkedlifedata.com/resource/pubmed/commentcorrection/6731437-953068
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
May
pubmed:issn
0002-9297
pubmed:author
pubmed:issnType
Print
pubmed:volume
36
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
623-33
pubmed:dateRevised
2009-11-18
pubmed:meshHeading
pubmed:year
1984
pubmed:articleTitle
Complementation of multiple sulfatase deficiency in somatic cell hybrids.
pubmed:publicationType
Journal Article, Research Support, U.S. Gov't, P.H.S., Research Support, Non-U.S. Gov't