Selective Isolation of Newly Synthesized Mammalian mRNA after in Vivo Labeling with 4-Thiouridine or 6-Thioguanosine (Record no. 44759)

MARC details
000 -LEADER
fixed length control field 02312nam a2200277Ia 4500
003 - CONTROL NUMBER IDENTIFIER
control field MX-MdCICY
005 - DATE AND TIME OF LATEST TRANSACTION
control field 20250625140633.0
040 ## - CATALOGING SOURCE
Transcribing agency CICY
090 ## - LOCALLY ASSIGNED LC-TYPE CALL NUMBER (OCLC); LOCAL CALL NUMBER (RLIN)
Classification number (OCLC) (R) ; Classification number, CALL (RLIN) (NR) B-10527
008 - FIXED-LENGTH DATA ELEMENTS--GENERAL INFORMATION
fixed length control field 250602s9999 xx |||||s2 |||| ||und|d
245 10 - TITLE STATEMENT
Title Selective Isolation of Newly Synthesized Mammalian mRNA after in Vivo Labeling with 4-Thiouridine or 6-Thioguanosine
490 0# - SERIES STATEMENT
Volume/sequential designation Analytical BioChemistry, 171(1), p.166-172, 1988
520 3# - SUMMARY, ETC.
Summary, etc. Newly synthesized mRNA from hamster cells was labeled in vivo with the thionucleoside analogs 4-thiouridine (4-TU)and 6-thioguanosine (6-TG). The thio-substituted RNA was selectively recovered by Affi-Gel 501 phenylmercury affinity chromatography. Following a l-h labeling period, enrichment for newly transcribed RNA after a single round of chromatography ranged between lo- and 15-fold when compared with total RNA. Exposure of CHO UrdA cells, a uridine auxotrophic line, to 50 pM 4-TLJ allowed for optimal recovery of newly transcribed RNA. Increasing the concentration of 4-TU to 100 pM or labeling with 6-TG at concentrations of 3 FM or greater resulted in similar recoveries from uridine-prototrophic hamster cell lines. For shorter term labeling, exposure of prototrophic cells to 500 fiM 4-TU or 100 pM 6-TG for 15 min allowed newly synthesized RNA to be selectively recovered. As a specific test case, enrichment for histone H3.2 mRNA was analyzed after hamster cells were labeled with 4-TU under conditions in which the gene was highly transcriptionally active. Northern blot analysis and the specific activity of thio-substituted RNA revealed a 15-fold enrichment when compared to total RNA. In vivo labeling of cellular RNA with 4-TU or 6-TG should provide a useful method for studying inducible gene expression and for isolating and cloning specific mRNAs from mammalian cells.
650 14 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element CHROMATOGRAPHY
650 14 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element NUCLEIC ACIDS
650 14 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element AFFINITY CHROMATOGRAPHY
650 14 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element RNA ISOLATION
650 14 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element HISTONE MRNA
650 14 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element 4-THIOURIDINE
650 14 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element 6-THIOGUANOSINE
700 12 - ADDED ENTRY--PERSONAL NAME
Personal name Woodford, T.
700 12 - ADDED ENTRY--PERSONAL NAME
Personal name Schlegel, R.
700 12 - ADDED ENTRY--PERSONAL NAME
Personal name Pardee, A.B.
856 40 - ELECTRONIC LOCATION AND ACCESS
Uniform Resource Identifier <a href="https://drive.google.com/file/d/1GlctxThmfEesJjvsgmJ6nq2vmYPct8DZ/view?usp=drivesdk">https://drive.google.com/file/d/1GlctxThmfEesJjvsgmJ6nq2vmYPct8DZ/view?usp=drivesdk</a>
Public note Para ver el documento ingresa a Google con tu cuenta: @cicy.edu.mx
942 ## - ADDED ENTRY ELEMENTS (KOHA)
Source of classification or shelving scheme Clasificación local
Koha item type Documentos solicitados
Holdings
Lost status Source of classification or shelving scheme Damaged status Not for loan Collection Home library Current library Shelving location Date acquired Total checkouts Full call number Date last seen Price effective from Koha item type
  Clasificación local     Ref1 CICY CICY Documento préstamo interbibliotecario 25.06.2025   B-10527 25.06.2025 25.06.2025 Documentos solicitados