Isolation, ultrastructure, and protein composition of the flagellar rootlet of Naegleria gruberi
نویسندگان
چکیده
Attached to the basal bodies of Naegleria gruberi flagellates is a striated rootlet or rhizoplast. The rootlet-basal body complex has been isolated by Triton X-100 lysis of deflagellated cells and differential centrifugation through a 25% glycerol medium. Rootlets isolated from mature flagellates are approximately 13 micrometers long but vary from 8 to 15 micrometers in length: they taper at both ends from a maximum width of approximately 0.25 micrometers in the vicinity of the basal bodies. They are highly stable during isolation but can be solubilized by urea, high salt, low pH, or detergent (Sarkosyl). Partial dissociation of rootlets with 1 M urea reveals that they are composed of filaments, approximately 5 nm diameter, associated in a linear fashion to yield the characteristic 21-nm cross-banded appearance. Differential solubilization of rootlets and their associated contaminants allowed identification of a major rootlet protein, comprising at least 50% of any purified rootlet preparation, with an apparent subunit molecular weight of 170,000. The localization of rootlets in situ by indirect immunofluorescence using a specific antibody directed against the purified rootlet protein demonstrated unequivocally that this 170,000-dalton protein is an organelle component.
منابع مشابه
Studies of the rhizoplast from Naegleria gruberi.
A procedure utilizing homogenization and centrifugation in a low ionic strength buffer containing Triton X-100, has been used to facilitate the isolation of the rhizoplast from flagellates of Naegleria gruberi. This has enabled a study to be made of the physical and biochemical properties of this organelle. The rhizoplast is shown to be a proteinaceous structure with chemical properties similar...
متن کاملPurification and properties of flagellar outer doublet tubulin from Naegleria gruberi and a radioimmune assay for tubulin.
Outer doublet tubulin has been purified from flagella of differentiated cells of the amebo-flagellate Naegleria gruberi. The flagellar tubulin is similar to other tubulins in molecular weight (55,000), amino acid composition, electrophoretic mobility, and nucleotide composition. However, the protein contains 2 moles of guanine nucleotide per 55,000 g of protein, twice that usually found in tubu...
متن کاملVariable Periodicity in the Rhizoplast of Naegleria Flagellates
Flagellar rootlets, rhizoplasts, and parabasal filaments are periodically banded structures which extend into the cytoplasm from the basal bodies and kinetosomes of flagella and cilia (Pitelka, 1969). In all but a few cases the banding pattern has been assumed to be constant for the rhizoplast of a particular organism. This note reports an electron microscope study of the banding pattern of the...
متن کاملmRNAs for alpha- and beta-tubulin and flagellar calmodulin are among those coordinately regulated when Naegleria gruberi amebae differentiate into flagellates
Three of four mRNAs that are specific to the differentiation of Naegleria gruberi amebae into flagellates (Mar, J., J. H. Lee, D. Shea, and C. J. Walsh, 1986, J. Cell Biol., 102:353-361) have been identified as coding for flagellar proteins. The products of these mRNAs, which are coordinately regulated during the differentiation, were identified by in vitro translation of hybrid-selected RNA fo...
متن کاملThe alpha-tubulin gene family expressed during cell differentiation in Naegleria gruberi
Genes that direct the programmed synthesis of flagellar alpha-tubulin during the differentiation of Naegleria gruberi from amebae to flagellates have been cloned, and found to be novel with respect to gene organization, sequence, and conservation. The flagellar alpha-tubulin gene family is represented in the genome by about eight homologous DNA segments that are exceptionally similar and yet ar...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
عنوان ژورنال:
- The Journal of Cell Biology
دوره 89 شماره
صفحات -
تاریخ انتشار 1981