Skip to main content
. 1998 Jun 1;12(11):1678–1690. doi: 10.1101/gad.12.11.1678

Table 2.

Composition of the purified RNase P holoenzyme and summary of functional analysis of each protein subunit

Gene
Subunit type
Estimated size (kd)
Processing defect with subunit depletion
Reduction of RNA with subunit depletion
Immunoprecipitated RNA
Referencea
pre-tRNA
pre-rRNA
pre-P
P
MRP
pre-P
P
MRP
RPR1 RNA 120 Lee et al. (1991)
POP1 protein 100.5 Y Y            Yb Y Y Y Y Y Lygerou et al. (1994)
POP4 protein 32.9 Y Y N Y Y Y Y Y Chu et al. (1997)
RPP1 protein 32.2 Y Y N Y Y Y Y Y Stolc and Altman (1997)
POP3 protein 22.6 Y Y N N N Y Y Y Dicht and Tollervey (1997)
POP5 protein 19.6 Y Y N Y Y Y Y Y this report
POP6 protein 18.2 Y Y N Y Y N N N this report
RPR2 protein 16.4 Y N N Y N Y Y N this report
POP7 protein 15.8 Y Y N Y Y Y N Y this report
POP8 protein 15.5 Y N N Y Y Y Y Y this report

(Y) Yes; (N) no; (pre) precursor. 

a

Information for Pop1p, Pop3p, Pop4p, and Rpp1p are derived from the references cited. The information reported for the remaining protein subunits is shown in Figs. 3 and 4

b

A pop1 temperature-sensitive strain was examined at a nonpermissive temperature for RNA reduction. Relative to the mature RNase P RNA the precursor RNase P RNA levels declined less rapidly, and it is unclear whether this depletion is a result of the general decline of functional RNA levels under this condition.