scholarly journals U1 small nuclear RNA genes are located on human chromosome 1 and are expressed in mouse-human hybrid cells.

1983 ◽  
Vol 3 (12) ◽  
pp. 2211-2220 ◽  
Author(s):  
E Lund ◽  
C Bostock ◽  
M Robertson ◽  
S Christie ◽  
J L Mitchen ◽  
...  

The majority, and perhaps all, of the genes for human U1 small nuclear RNA (U1 RNA) were shown to be located on the short arm of human chromosome 1. These genes were mapped by Southern blot analysis of DNA from rodent-human somatic cell hybrids, using the 5' region of a human U1 RNA gene as a human-specific probe. This probe hybridized to DNA fragments present only in digests of total human DNA or to the DNAs of cell lines which contained human chromosome 1. The major families of human U1 RNA genes were identified, but some human genes may have gone undetected. Also, the presence of a few U1 RNA genes on human chromosome 19 could not be ruled out. In spite of the lack of extensive 5'-flanking-region homology between the human and mouse U1 RNA genes, the genes of both species were efficiently transcribed in the hybrid cells, and the U1 RNAs of both species were incorporated into specific ribonucleoprotein particles.

1983 ◽  
Vol 3 (12) ◽  
pp. 2211-2220
Author(s):  
E Lund ◽  
C Bostock ◽  
M Robertson ◽  
S Christie ◽  
J L Mitchen ◽  
...  

The majority, and perhaps all, of the genes for human U1 small nuclear RNA (U1 RNA) were shown to be located on the short arm of human chromosome 1. These genes were mapped by Southern blot analysis of DNA from rodent-human somatic cell hybrids, using the 5' region of a human U1 RNA gene as a human-specific probe. This probe hybridized to DNA fragments present only in digests of total human DNA or to the DNAs of cell lines which contained human chromosome 1. The major families of human U1 RNA genes were identified, but some human genes may have gone undetected. Also, the presence of a few U1 RNA genes on human chromosome 19 could not be ruled out. In spite of the lack of extensive 5'-flanking-region homology between the human and mouse U1 RNA genes, the genes of both species were efficiently transcribed in the hybrid cells, and the U1 RNAs of both species were incorporated into specific ribonucleoprotein particles.


1977 ◽  
Vol 25 (1) ◽  
pp. 39-57 ◽  
Author(s):  
S.J. Goss ◽  
H. Harris

A method is described which should permit determination of the order and spacing of genes on all human chromosomes by the analysis of just one set of man-mouse hybrid cells. This method is used to determine the map of 8 loci on human chromosome I. A comparison of the statistical maps of chromosome I and of the X-chromosome with the cytogenetic maps of these chromosomes at metaphase indicates that the statistically derived distances between genes are related to the amount of Giemsa light-band material between the genes.


1984 ◽  
Vol 10 (3) ◽  
pp. 307-313 ◽  
Author(s):  
S. L. Naylor ◽  
B. U. Zabel ◽  
T. Manser ◽  
R. Gesteland ◽  
A. Y. Sakaguchi

1985 ◽  
Vol 5 (9) ◽  
pp. 2172-2180 ◽  
Author(s):  
V Lindgren ◽  
L B Bernstein ◽  
A M Weiner ◽  
U Francke

Human U1 small nuclear RNA is encoded by approximately 30 gene copies. All of the U1 genes share several kilobases of essentially perfect flanking homology both upstream and downstream from the U1 coding region, but remarkably, for many U1 genes excellent flanking homology extends at least 24 kilobases upstream and 20 kilobases downstream. Class I U1 RNA pseudogenes are abundant in the human genome. These pseudogenes contain a complete but imperfect U1 coding region and possess extensive flanking homology to the true U1 genes. We mapped four class I pseudogenes by in situ hybridization to the long arm of chromosome 1, bands q12-q22, a region distinct from the site on the distal short arm of chromosome 1 to which the U1 genes have been previously mapped (Lund et al., Mol. Cell. Biol. 3:2211-2220, 1983; Naylor et al., Somat. Cell Mol. Genet. 10:307-313, 1984). We confirmed our in situ hybridization results by genomic blotting experiments with somatic cell hybrid lines with translocation products of human chromosome 1. These experiments provide further evidence that class I U1 pseudogenes and the true U1 genes are not interspersed. The results, along with those published elsewhere (Bernstein et al., Mol. Cell. Biol. 5:2159-2171, 1985), suggest that gene amplification may be responsible for the sequence homogeneity of the human U1 gene family.


1975 ◽  
Vol 15 (1) ◽  
pp. 50-54 ◽  
Author(s):  
K.C. Atwood ◽  
M.T. Yu ◽  
L.D. Johnson ◽  
A.S. Henderson

1985 ◽  
Vol 5 (9) ◽  
pp. 2172-2180 ◽  
Author(s):  
V Lindgren ◽  
L B Bernstein ◽  
A M Weiner ◽  
U Francke

Human U1 small nuclear RNA is encoded by approximately 30 gene copies. All of the U1 genes share several kilobases of essentially perfect flanking homology both upstream and downstream from the U1 coding region, but remarkably, for many U1 genes excellent flanking homology extends at least 24 kilobases upstream and 20 kilobases downstream. Class I U1 RNA pseudogenes are abundant in the human genome. These pseudogenes contain a complete but imperfect U1 coding region and possess extensive flanking homology to the true U1 genes. We mapped four class I pseudogenes by in situ hybridization to the long arm of chromosome 1, bands q12-q22, a region distinct from the site on the distal short arm of chromosome 1 to which the U1 genes have been previously mapped (Lund et al., Mol. Cell. Biol. 3:2211-2220, 1983; Naylor et al., Somat. Cell Mol. Genet. 10:307-313, 1984). We confirmed our in situ hybridization results by genomic blotting experiments with somatic cell hybrid lines with translocation products of human chromosome 1. These experiments provide further evidence that class I U1 pseudogenes and the true U1 genes are not interspersed. The results, along with those published elsewhere (Bernstein et al., Mol. Cell. Biol. 5:2159-2171, 1985), suggest that gene amplification may be responsible for the sequence homogeneity of the human U1 gene family.


Nature ◽  
1974 ◽  
Vol 252 (5485) ◽  
pp. 741-743 ◽  
Author(s):  
DALE M. STEFFENSEN ◽  
P. DUFFEY ◽  
W. PRENSKY

2002 ◽  
Vol 33 (2) ◽  
pp. 91-96 ◽  
Author(s):  
H. S. Sun ◽  
C. K. Tuggle ◽  
A. Goureau ◽  
C. J. Fitzsimmons ◽  
P. Pinton ◽  
...  

Nature ◽  
2006 ◽  
Vol 443 (7114) ◽  
pp. 1013-1013
Author(s):  
S. G. Gregory ◽  
K. F. Barlow ◽  
K. E. McLay ◽  
R. Kaul ◽  
D. Swarbreck ◽  
...  

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