1996
DOI: 10.1083/jcb.135.1.1
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A unified nomenclature for peroxisome biogenesis factors.

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Cited by 368 publications
(213 citation statements)
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“…This possibility was excluded by examining the ability of cells totally lacking peroxisomes to sporulate on this medium type. S. cerevisiae ⌬pex6 (formerly pas8; Voorn-Brouwer et al, 1993;Distel et al, 1996) mutant cells (yAG176) are devoid of peroxisomes showing no detectable peroxisomal structures. The homozygous ⌬pex6 diploid strain sporulated to wild-type levels of over 50% on solid medium containing acetate, and we therefore reasoned that, in S. cerevisiae, meiotic development takes place in the total absence of peroxisomal structures that may contain an intact ␤-oxidation system.…”
Section: Pip2p and Oaf1p Are Not Required For Sporulationmentioning
confidence: 99%
“…This possibility was excluded by examining the ability of cells totally lacking peroxisomes to sporulate on this medium type. S. cerevisiae ⌬pex6 (formerly pas8; Voorn-Brouwer et al, 1993;Distel et al, 1996) mutant cells (yAG176) are devoid of peroxisomes showing no detectable peroxisomal structures. The homozygous ⌬pex6 diploid strain sporulated to wild-type levels of over 50% on solid medium containing acetate, and we therefore reasoned that, in S. cerevisiae, meiotic development takes place in the total absence of peroxisomal structures that may contain an intact ␤-oxidation system.…”
Section: Pip2p and Oaf1p Are Not Required For Sporulationmentioning
confidence: 99%
“…4). Pex11p may function as a peroxisome biogenesis regulator, possibly by interacting with other PEX proteins [2,3,18], including RING peroxins, Pex2p [13,22,46] and Pex12p [15,16,27], AAA family peroxins Pex1p [17,19,20] and Pex6p [14,25,26], a tetratricopeptide repeat (TPR) protein Pex5p (PTS1 receptor) [23,24,47], a WD motif protein Pex7p (PTS2 receptor) [48^50], and Pex13p (PTS1 receptor docking protein) presumed in mammals [51]. Functional role of Pex11p in peroxisome biogenesis in mammals remains to be investigated.…”
Section: Intracellular Localization and Topology Of Pex11pmentioning
confidence: 99%
“…Peroxisomes are formed by division of preexisting peroxisomes after posttranslational import of newly synthesized proteins [1]. Genetic analysis of peroxisome-de¢cient mutants of yeast and mammalian cells have led to identi¢cation of a number of protein factors essential for peroxisome biogenesis [2,3]. Genetical heterogeneities comprising 12 complementation groups (CGs) have been identi¢ed in mammals, including humans [4^12].…”
Section: Introductionmentioning
confidence: 99%
“…Two distinct topogenic signals, peroxisomal targeting signal type 1 (PTS1) and PTS2 (16,40), direct proteins to the peroxisomal matrix. Genetic analyses of peroxisome-deficient mutants isolated from yeast and mammalian cells led to the identification of a number of proteins, known as peroxins, which are essential for peroxisome biogenesis (11,17,23,41). PEX5 and PEX7 encode the receptors for PTS1 and PTS2, respectively.…”
mentioning
confidence: 99%