1992
DOI: 10.1128/mcb.12.4.1460
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Reconstitution of functional mammalian U4 small nuclear ribonucleoprotein: Sm protein binding is not essential for splicing in vitro.

Abstract: We have developed an in vitro splicing complementation assay to investigate the domain structure of the mammalian U4 small nuclear RNA (snRNA) through mutational analysis. The addition of affinity-purified U4 snRNP or U4 RNA to U4-depleted nuclear extract efficiently restores splicing activity. In the U4-U6 interaction domain of U4 RNA, only stem II was found to be essential for splicing activity; the 5' loop is important for spliceosome stability. In the central domain, we have identified a U4 RNA sequence el… Show more

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Cited by 36 publications
(28 citation statements)
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“…Regardless, Hahn et al (2012) found that the 39 SL alone does not bind Brr2, implying that other RNA parts are required, and MozaffariJovin et al (2012) showed that the central domain of U4 plays a key role in Brr2 binding as well as in U4/U6 unwinding. Consistent with an important role for the central domain, bases in this domain adjacent to stem I have been shown to be important for splicing (Wersig and Bindereif 1992). Notably, however, the central domain of U4 can be endonucleolytically cleaved after formation of U4/U6 with little consequence for splicing (Hayduk et al 2012).…”
Section: Does the 39 Region Of U4 Position Brr2 For Unwinding?mentioning
confidence: 74%
“…Regardless, Hahn et al (2012) found that the 39 SL alone does not bind Brr2, implying that other RNA parts are required, and MozaffariJovin et al (2012) showed that the central domain of U4 plays a key role in Brr2 binding as well as in U4/U6 unwinding. Consistent with an important role for the central domain, bases in this domain adjacent to stem I have been shown to be important for splicing (Wersig and Bindereif 1992). Notably, however, the central domain of U4 can be endonucleolytically cleaved after formation of U4/U6 with little consequence for splicing (Hayduk et al 2012).…”
Section: Does the 39 Region Of U4 Position Brr2 For Unwinding?mentioning
confidence: 74%
“…Wersig and Bindereif (1992) showed that a human U4 snRNA mutant, whose Sm core site was mutated such as to abolish immunoprecipitation with anti-Sm antibodies, was active in an in vitro splicing complementation assay. This result suggests that the common proteins bound to U4 snRNA play no essential role in splicing in vitro.…”
Section: Discussionmentioning
confidence: 99%
“…Neither the m 3 G cap nor internal modifications are essential for the function of U1 , U4 (Wersig and Bindereif 1992), U5 (Ségault et al 1995), or U6 (Wolff and Bindereif 1992) snRNAs in splicing in vitro. In contrast, post-transcriptional modifications are essential for U2 function in Xenopus oocytes (Pan and Prives 1989) and HeLa nuclear extract (Ségault et al 1995), but their role remains poorly understood.…”
Section: Introductionmentioning
confidence: 99%