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Molecular and Cellular Biology, February 2000, p. 1055-1062, Vol. 20, No. 3
Max Planck Institut für
Biochemie1 and Max Planck Institut
für Neurobiologie,3 82152 Martinsried,
Germany, and Department of Experimental Pathology, Lund
University, 221 85 Lund, Sweden2
Received 1 October 1999/Accepted 13 October 1999
Small nuclear ribonucleoproteins (snRNPs) are particles present
only in eukaryotic cells. They are involved in a large variety of RNA
maturation processes, most notably in pre-mRNA splicing. Several of the
proteins typically found in snRNPs contain a sequence signature, the Sm
domain, conserved from yeast to mammals. By using a promoter trap
strategy to target actively transcribed loci in murine embryonic stem
cells, a new murine gene encoding an Sm motif-containing protein was
identified. Database searches revealed that it is the mouse orthologue
of Lsm4p, a protein found in yeast and human cells and putatively
associated with U6 snRNA. Introduction of the geo reporter
gene cassette under the control of the murine Lsm4
(mLsm4) endogenous promoter showed that the gene was
ubiquitously transcribed in embryonic and adult tissues. The insertion
of the geo cassette disrupted the mLsm4 allele, and homozygosity for the mutation led to a recessive embryonic lethal
phenotype. mLsm4-null zygotes survived to the blastocyst stages,
implanted into the uterus, but died shortly thereafter. The early death
of mLsm4p-null mice suggests that the role of mLsm4p in splicing is
essential and cannot be compensated by other Lsm proteins.
0270-7306/00/$04.00+0
Copyright © 2000, American Society for Microbiology. All rights reserved.
Peri-Implantation Lethality in Mice Lacking the Sm
Motif-Containing Protein Lsm4

*
Corresponding author. Mailing address: Department of
Experimental Pathology, Lund University, S-22185 Lund, Sweden. Phone: 46-46-173-553. Fax: 46-46-158-202. E-mail:
reinhard.fassler{at}pat.lu.se.
Present address: Dipartimento di Genetica, Biologia e Biochimica,
Università di Torino, Turin, Italy.
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