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1.
ABSTRACT. The microtubules of the amitochondrial parasite Entamoeba histolytica are atypical in certain respects. Consistent with this, we report that E. histolytica encodes the most divergent β -tubulin identified to date, with only 54% to 58% identity to β -tubulins from various species. A similarly divergent β -tubulin is encoded by the related Entamoeba invadens ; single gene copies appear to be present in both organisms. The Entamoeba sequences were compared with a database of 101 β -tubulins, including the highly divergent sequence from another amitochondrial protozoan, Trichomonas vaginalis. A total of 81 residues were universally conserved, and 76 residues varied only once. Correlations with previous studies indicate that microtubule function is altered when most, but not all, conserved residues are mutated. 相似文献
2.
Koga-Ban Yasunori; Niki Tomoya; Nagamura Yoshiaki; Sasaki Takuji; Minobe Yuzo 《DNA research》1995,2(1):21-26
Complete nucleotide sequences of three kinds of rice ß-tubulincDNA clones (pTUB22, R1623 and R2242) were determined. Southernhybridization indicated that these ß-tubulins consistof one gene family. Using RFLP mapping, these three ß-tubulincDNAs were mapped to different chromosomes indicating at leastthree loci for the ß-tubulin gene. The deduced aminoacid sequences of these cDNAs showed a high similarity to otherplant ß-tubulins. The asparagine residue located atthe 100th amino acid from the Nterminus of plant ß-tubulinswas also conserved with these three ß-tubulins. Thisasparagine is thought to be responsible for the sensitivityagainst rhizoxin, the toxin of the pathogen of rice seedlingblight, Rhizopus sp. a soil-borne microorganism. Expressionof the three ß-tubulin genes was analyzed by Northernblotting and all three clones were expressed in root, the possibletarget tissue of rhizoxin. These results suggest that theseclones are candidates of ß-tubulins targeted by rhizoxin. 相似文献
3.
Mark J. Guiltinan Din Pow Ma Richard F. Barker Mauricio M. Bustos Richard J. Cyr Ramin Yadegari Donald E. Fosket 《Plant molecular biology》1987,10(2):171-184
Two divergent -tubulin genes (designated S-1 and S-2) were isolated by screening a soybean genomic library with a Chlamydomonas reinhardtii -tubulin cDNA probe. Restriction fragment analysis of the clones recovered, and of soybean genomic DNA, indicated that these represent two unique classes of structurally different -tubulin genes in the soybean genome. However, it is possible that unidentified members of these classes or additional highly divergent classes of -tubulin genes (thus far undetected) exist in the soybean genome. The S-1 and S-2 genomic clones were sequenced, revealing that both are potentially functional genes which would encode -tubulins of 445 and 449 amino acids, respectively. A comparison of their derived amino acid sequences with -tubulins from several organisms showed that they are most homologous to Chlamydomonas -tubulin (85–87%), with lesser degrees of homology to -tubulins of vertebrate species (79–83%), Trypanosoma brucei (80–81%) and Saccharomyces cerevisiae (66–68%). The amino acid sequences of S-1 and S-2 are as divergent from each other as they are from the Chlamydomonas -tubulin. The amino acids at the diverged positions in S-2 are nearly all conservative substitutions while in S-1, 18 of the 69 substitutions were non-conservative. Both soybean -tubulin genes contain two introns in exactly the same positions. The first soybean intron is located in the same position as the third intron of the Chlamydomonas -tubulin genes. Codon usage in the two soybean -tubulins is remarkably similar (D
2=0.87), but differs from codon usage in other soybean genes. 相似文献
4.
5.
Andrey Smertenko Yaroslav Blume Vladimír Viklický Zdeněk Opatrný Pavel Dráber 《Planta》1997,201(3):349-358
Distribution of post-translationally modified tubulins in cells of Nicotiana tabacum L. was analysed using a panel of specific antibodies. Polyglutamylated, tyrosinated, nontyrosinated, acetylated and Δ2-tubulin
variants were detected on α-tubulin subunits; polyglutamylation was also found on β-tubulin subunits. Modified tubulins were
detected by immunofluorescence microscopy in interphase microtubules, preprophase bands, mitotic spindles as well as in phragmoplasts.
They were, however, located differently in the various microtubule structures. The antibodies against tyrosinated, acetylated
and polyglutamylated tubulins gave uniform staining along all microtubules, while antibodies against nontyrosinated and Δ2-tubulin
provided dot-like staining of interphase microtubules. Additionally, immunoreactivity of antibodies against acetylated and
Δ2-tubulins was strong in the pole regions of mitotic spindles. High-resolution isoelectric focusing revealed 22 tubulin charge
variants in N. tabacum suspension cells. Immunoblotting with antibodies TU-01 and TU-06 against conserved antigenic determinants of α- and β-tubulin
molecules, respectively, revealed that 11 isoforms belonged to the α-subunit and 11 isoforms to the β-subunit. Whereas antibodies
against polyglutamylated, tyrosinated and acetylated tubulins reacted with several α-tubulin isoforms, antibodies against
nontyrosinated and Δ2-tubulin reacted with only one. The combined data demonstrate that plant tubulin is extensively post-translationally
modified and that these modifications participate in the generation of plant tubulin polymorphism.
Received: 2 May 1996 / Accepted: 16 September 1996 相似文献
6.
The anti-cancer drug taxol binds to β-tubulin in assembled microtubules and causes cell cycle arrest in animal cells; in
contrast, in fungi, the effect of taxol varies. For instance, the taxol-producer Pestalotiopsis microspora Ne32, an ascomycete, is resistant to taxol (IC50 greater than 11.7 μM), whereas Pythium ultimum, an oomycete, is sensitive to taxol (IC50 0.1 μM). In order to understand the differential fungal response to taxol, we isolated cDNAs encoding β-tubulin from both
P. microspora and P. ultimum. The deduced amino acid sequence of β-tubulin from P. microspora is very similar to those from other Ascomycetes, many of which are resistant to taxol. The sequence of β-tubulin from P. ultimum is very similar to those from Oomycetes and non-fungal organisms, many of which are sensitive to taxol. To examine the interaction
between taxol and fungal microtubules, binding studies were performed with fungal cells, using [3H]taxol. The labeled taxol was found to bind specifically to P. ultimum, but not to P. microspora. In addition, the amount of [3H]taxol specifically bound to P. ultimum was reduced by the microtubule-depolymerizing drug thiabendazole, in a dose-dependent manner. These results suggest efficient
binding of taxol to microtubules in P. ultimum, but not in P. microspora, and are consistent with the differential taxol sensitivity of these two organisms. Finally a comparison of previously characterized
taxol binding sites in various β-tubulin sequences showed that β-tubulins of taxol-sensitive organisms, including P. ultimum, contain Thr219, but β-tubulins of resistant organisms, including P. microspora, contain Asn or Gln at this position, suggesting an important role for residue 219 in the interaction between taxol and β-tubulin.
Received: 16 March 1999 / Accepted: 21 August 1999 相似文献
7.
Distinct localization of a beta-tubulin epitope in the Tetrahymena thermophila and Paramecium caudatum cortex 总被引:1,自引:0,他引:1
Summary. Many of the highly organized microtubular arrangements in ciliates are located in the cortical area containing membrane vesicles
and vacuoles. In Tetrahymena thermophila and Paramecium caudatum, immunofluorescence microscopy with the monoclonal antibody TU-06, directed against β-tubulin, revealed distinct staining
of this cortical region alone, while the cilia and other microtubular structures were unstained. The specificity of the antibody
was confirmed by immunoblotting and by preabsorption of the antibody with purified tubulin. Double-label immunofluorescence
with antibodies against γ-tubulin, detyrosinated α-tubulin, and centrin showed that the TU-06 epitope is localized outside
the basal body region. This was also confirmed by immunogold electron microscopy of thin sections. Proteolytic digestion of
porcine brain β-tubulin combined with a peptide scan of immobilized, overlapping peptides disclosed that the epitope was in
the β-tubulin region β81–95, a region which is phylogenetically highly conserved. As known posttranslational modifications
of β-tubulin are located outside this area, the observed staining pattern cannot be interpreted as evidence of subcellular
sequestration of modified tubulin. The limited distribution of the epitope could rather reflect the dependence of TU-06 epitope
exposition on conformations of tubulin molecules in microtubule arrangements or on differential masking by interacting proteins.
Correspondence and reprints: Institute of Molecular Genetics, Czech Academy of Sciences, Vídeňská 1083, 14220 Prague, Czech
Republic. 相似文献
8.
A Colcemid-resistant Chinese hamster line with an altered form of β-tubulin was used in studies of the expression of spindle
proteins in interspecific cell hybrids. Eight hybrids between this line, and a Colcemid-sensitive mouse cell line, were studied.
The altered hamster β-tubulin was not expressed as an increased resistance to Colcemid in any hybrid. Since the complete hamster
chromosome complement was represented among the hybrids, the absence of altered β-tubulin is not due to segregation of the
mutant hamster β-tubulin gene. We suggest either that the hamster β-tubulin gene is repressed in hybrids, or that hamster
β-tubulin is excluded from the spindle in hybrid cells. We compare these findings with previous reports of the repression
of other highly active, moderately repeated constitutive genes in interspecific hybrids. 相似文献
9.
Summary Antibodies specific to five different maize isotubulins were made. From predicted amino acid sequences established from previously sequenced maize tubulin genes, peptide antigens were synthesized matching the carboxyl-terminal 11–13 amino acids of each of three maize -tubulins and two maize -tubulins. Antibodies were generated by injecting conjugated antigens into hens, collecting their eggs, and extracting immunoglobulin Y from the egg yolk. Specificity of each antibody was tested by immunoblotting of fusion proteins containing the antigenic sequence of the specific - and -tubulin isoforms. For all five isotubulins, antibodies were affinity-purified with fusion proteins corresponding to their respective antigens, to remove nonspecific binding found in the antibody preparations. Further preparation of anti--tubulins was required to eliminate cross-reactivity of antibodies with members of other -tubulin subfamilies. For this, affinity-purified antibodies against a specific -tubulin were preadsorbed with peptides representing cross-reactive -tubulin antigens. Results indicated that virtually all cross-reactivity between members of different -tubulin subfamilies could be eliminated, resulting in labeling of only the fusion protein containing the specific antigen. All five isotubulin antibodies generated showed labeling of discrete spots on two-dimensional immunoblots of maize proteins, demonstrating the specificity of the antibodies in complex tubulin mixtures. These antibodies should prove valuable for analyzing the developmental distribution, and possible functional significance, of several maize isotubulins.Abbreviations BSA
bovine serum albumin
- 2-D
two-dimensional
- GCG
Genetics Computer Group
- Ig
Immunoglobulin
- KLH
keyhole limpet hemocyanin
- PBS
phosphate-buffered saline
- PVDF
polyvinylidene-difluoride
- SDS-PAGE
sodium dodecyl sulfate-poly-acrylamide gel electrophoresis
- TBS
Tris-buffered saline
- TE
Tris EDTA buffer 相似文献
10.
We have determined the lesions in a number of mutant alleles of βTub85D, the gene that encodes the testis-specific β2-tubulin isoform in Drosophila melanogaster. Mutations responsible for different classes of functional phenotypes are distributed throughout the β2-tubulin molecule. There is a telling correlation between the degree of phylogenetic conservation of the altered residues and the number of different microtubule categories disrupted by the lesions. The majority of lesions occur at positions that are evolutionarily highly conserved in all β-tubulins; these lesions disrupt general functions common to multiple classes of microtubules. However, a single allele B2t(6) contains an amino acid substitution within an internal cluster of variable amino acids that has been identified as an isotype-defining domain in vertebrate β-tubulins. Correspondingly, B2t(6) disrupts only a subset of microtubule functions, resulting in misspecification of the morphology of the doublet microtubules of the sperm tail axoneme. We previously demonstrated that β3, a developmentally regulated Drosophila β-tubulin isoform, confers the same restricted morphological phenotype in a dominant way when it is coexpressed in the testis with wild-type β2-tubulin. We show here by complementation analysis that β3 and the B2t(6) product disrupt a common aspect of microtubule assembly. We therefore conclude that the amino acid sequence of the β2-tubulin internal variable region is required for generation of correct axoneme morphology but not for general microtubule functions. As we have previously reported, the β2-tubulin carboxy terminal isotype-defining domain is required for suprastructural organization of the axoneme. We demonstrate here that the β2 variant lacking the carboxy terminus and the B2t(6) variant complement each other for mild-to-moderate meiotic defects but do not complement for proper axonemal morphology. Our results are consistent with the hypothesis drawn from comparisons of vertebrate β-tubulins that the two isotype-defining domains interact in a three-dimensional structure in wild-type β-tubulins. We propose that the integrity of this structure in the Drosophila testis β2-tubulin isoform is required for proper axoneme assembly but not necessarily for general microtubule functions. On the basis of our observations we present a model for regulation of axoneme microtubule morphology as a function of tubulin assembly kinetics. 相似文献
11.
A. I. Yemets W. V. Baird A. Yu. Nyporko G. A. Swire-Clark Ya. B. Blume 《Cytology and Genetics》2009,43(5):352-359
The identification of the location of a point mutation on β-tubulin molecules of amiprophosmethyland trifluralin-resistant
Nicotiana plumbaginifolia lines are described in this work. It was shown that in the first case, this mutation is related with the substitution of
serine residue for proline in position 248; in the second case, with the substitution of phenylalanine for serine in position
317 of the β-tubulin’s amino acid sequence. Three-dimensional models of the β-tubulin molecule from Chlamydomonas with the well-known location of mutations determining dinitroaniline- and phosphorothioamides resistance (the substitution
of lysine residue for methionine in position 350), and β-tubulin from Nicotiana plumbagnifolia have been reconstructed. On the basis of the analysis of the interaction site for dinitroanilines and phosphorothioamides
located on the Chlamydomonas β-tubulin’s molecule it was concluded that the revealed mutations on Nicotiana plumbaginifolia β-tubulin are affected by the residues of the amino acids, participating in the formation of this site. 相似文献
12.
In maturing seed cells, proteins that accumulate in the protein storage vacuoles (PSVs) are synthesized on the endoplasmic reticulum (ER) and transported by vesicles to the PSVs. Vacuolar sorting determinants (VSDs) which are usually amino acid sequences of short or moderate length direct the proteins to this pathway. VSDs identified so far are classified into two types: sequence specific VSDs (ssVSDs) and C-terminal VSDs (ctVSDs). We previously demonstrated that VSDs of α′ and β subunits of β-conglycinin, one of major storage proteins of soybean (Glycine max), reside in the C-terminal ten amino acids. Here we show that both types of VSDs coexist within this region of the α′ subunit. Although ctVSDs can function only at the very C-termini of proteins, the C-terminal ten amino acids of α′ subunit directed green fluorescent protein (GFP) to the PSVs even when they were placed at the N-terminus of GFP, indicating that an ssVSD resides in the sequence. By mutation analysis, it was found that the core sequence of the ssVSD is Ser-Ile-Leu (fifth to seventh residues counted from the C-terminus) which is conserved in the α and β subunits and some vicilin-like proteins. On the other hand, the sequence composed of the C-terminal three amino acids (AFY) directed GFP to the PSVs when it was placed at the C-terminus of GFP, though the function as a VSD was disrupted at the N-terminus of GFP, indicating that the AFY sequence is a ctVSD. 相似文献
13.
E. Dráberová Zdenek Lukás Dagmar Ivanyi Vladimír Viklický Pavel Dráber 《Histochemistry and cell biology》1998,109(3):231-239
The class III β-tubulin isotype is widely used as a neuronal marker in normal and neoplastic tissues. This isotype was, however,
also immunodetected in certain tumours of non-neuronal origin such as squamous cell carcinoma. Using a newly described monoclonal
antibody we compared the distribution of class III β-tubulin in normal and neoplastic tissues. The TU-20 mouse monoclonal
antibody was prepared against a conserved synthetic peptide from the C-terminus of the human class III β-tubulin isotype,
and its specificity was confirmed by immunoblotting, by competitive enzyme-linked immunosorbent assay and by immunofluorescence
microscopy on cultured cells. In different cell lines of various origins the antibody reacted only with neuroblastoma Neuro-2a
cells and with embryonal carcinoma P19 cells stimulated to neuronal differentiation by retinoic acid. Immunohistochemistry
on formaldehyde-fixed paraffin-embedded normal human tissues revealed the presence of the class III β-tubulin isotype in cell
bodies and processes of neuronal cells in the peripheral and central nervous systems. In other tissues, this β-tubulin isotype
was not immunodetected. Class III β-tubulin was found in all cases of ganglioneuroblastoma, ganglioneuroma, medulloblastoma,
neuroblastoma, sympathoblastoma and in one case of teratoma. In contrast, no reactivity was detected in tumours of non-neuronal
origin, including 32 cases of squamous cell carcinoma. The results indicate a specific TU-20 epitope expression exclusively
in neuronal tissues. The antibody could thus be a useful tool for the probing of class III β-tubulin functions in neurons
as well as for immunohistochemical characterisation of tumours of neuronal origin.
Accepted: 29 July 1997 相似文献
14.
应用两对引物,从对多菌灵具有耐药性的链格孢属3个真菌中扩增了与多菌灵耐药性相关的β-微管蛋白基因,基因长度分别为1,419bp(瓜链格孢),1,426bp(茄链格孢),1,419bp(链格孢),均包含3个内含子,编码398个氨基酸。3个链格孢属真菌与其他对多菌灵敏感的植物病原真菌β-微管蛋白氨基酸具有高度的同源性。但是,3个真菌167位氨基酸均为酪氨酸,而其他对多菌灵敏感的真菌167位均为苯丙氨酸,研究结果表明链格孢属真菌对多菌灵的耐药性可能与167位酪氨酸有关。 相似文献
15.
This paper reports on the isolation of a cDNA clone ( tba-6 ) encoded by a novel a-tubulin gene in the nematode C. elegans . The tba-6 gene is located on chromosome I, that encode a protein of 460 amino acids, as well as the expression of the gene during the development. Here we discuss the structure of the coding region and the regulatory sequences in the promoter region. The comparison of the amino acid sequence of TBA6 with other α-tubulin isotypes of C. elegans , suggests that these proteins are highly conserved in most of the N-terminal and intermediate sequence, but they have highly divergent C-terminal sequences. TBA6 has also high homology with other α-tubulin families (e.g. human, mouse, Drosophila melangaster ). The in situ experiment results suggest that the tba-6 α-tubulin gene is required during the entire embryonic development, therefore it is required during the early cell division stages. Further, we determined the 3D structure of C. elegans TBA6 α-tubulin by altering (computationally) the crystal structure of the α-tubulin (TBA_pig) from porcine α-β tubulin dimer. We discuss structural conservation and changes in the pattern of interactions between secondary structure elements of TBA_pig and TBA6, respectively. 相似文献
16.
Bon-Sung Koo Satish Kalme Soo-Hwan Yeo Su-Jae Lee Moon-Young Yoon 《Plant Physiology and Biochemistry》2009,47(9):761-768
Few studies have investigated microtubules from plants that host pathogenic fungi. Considerable efforts are underway to find an antimitotic agent against plant pathogens like Phytophthora infestans. However, screening the effects of antifungal agents on plant tubulin in vivo or using purified native microtubule in vitro is a time consuming process. A recombinant, correctly folded, microtubule-like structure forming tubulin could accelerate research in this area. In this study, we cloned full length cDNAs isolated from potato leaves using reverse-transcribed polymerase chain reaction (RT-PCR). Solanum tuberosum (Stub) α-tubulin and β-tubulin were predicted to encode 449 and 451 amino acid long proteins with molecular masses of 57 kDa and 60 kDa, respectively. Average yields of α- and β-tubulin were 2.0–3.5 mg l?1 and 1.3–3.0 mg l?1 of culture, respectively. The amino acids, His6, Glu198, and Phe170 involved in benomyl sensitivity were conserved in Stub tubulin. The dimerization of tubulin monomers was confirmed by western blot analysis. When combined under appropriate conditions, these recombinant α- and β-tubulins were capable of polymerizing into microtubules. Accessibility of cysteine residues of tubulin revealed that important ligand binding sites were folded correctly. This recombinant tubulin could serve as a control of phytotoxicity of selected antimitotic fungicide compounds during in vitro screening experiments. 相似文献
17.
Structures of homologous proteins are usually conserved during evolution, as are critical active site residues. This is the
case for actin and tubulin, the two most important cytoskeleton proteins in eukaryotes. Actins and their related proteins
(Arps) constitute a large superfamily whereas the tubulin family has fewer members. Unaligned sequences of these two protein
families were analysed by searching for short groups of family-specific amino acid residues, that we call motifs, and by counting
the number of residues from one motif to the next. For each sequence, the set of motif-to-motif residue counts forms a subfamily-specific
pattern (landmark pattern) allowing actin and tubulin superfamily members to be identified and sorted into subfamilies. The
differences between patterns of individual subfamilies are due to inserts and deletions (indels). Inserts appear to have arisen
at an early stage in eukaryote evolution as suggested by the small but consistent kingdom-dependent differences found within
many Arp subfamilies and in γ-tubulins. Inserts tend to be in surface loops where they can influence subfamily-specific function
without disturbing the core structure of the protein. The relatively few indels found for tubulins have similar positions
to established results, whereas we find many previously unreported indel positions and lengths for the metazoan Arps. 相似文献
18.
Martha H. Stipanuk Chad R. Simmons P. Andrew Karplus John E. DominyJr. 《Amino acids》2011,41(1):91-102
Proteins in the cupin superfamily have a wide range of biological functions in archaea, bacteria and eukaryotes. Although
proteins in the cupin superfamily show very low overall sequence similarity, they all contain two short but partially conserved
cupin sequence motifs separated by a less conserved intermotif region that varies both in length and amino acid sequence.
Furthermore, these proteins all share a common architecture described as a six-stranded β-barrel core, and this canonical
cupin or “jelly roll” β-barrel is formed with cupin motif 1, the intermotif region, and cupin motif 2 each forming two of
the core six β-strands in the folded protein structure. The recently obtained crystal structures of cysteine dioxygenase (CDO),
with contains conserved cupin motifs, show that it has the predicted canonical cupin β-barrel fold. Although there had been
no reports of CDO activity in prokaryotes, we identified a number of bacterial cupin proteins of unknown function that share
low similarity with mammalian CDO and that conserve many residues in the active-site pocket of CDO. Putative bacterial CDOs
predicted to have CDO activity were shown to have similar substrate specificity and kinetic parameters as eukaryotic CDOs.
Information gleaned from crystal structures of mammalian CDO along with sequence information for homologs shown to have CDO
activity facilitated the identification of a CDO family fingerprint motif. One key feature of the CDO fingerprint motif is
that the canonical metal-binding glutamate residue in cupin motif 1 is replaced by a cysteine (in mammalian CDOs) or by a
glycine (bacterial CDOs). The recent report that some putative bacterial CDO homologs are actually 3-mercaptopropionate dioxygenases
suggests that the CDO family may include proteins with specificities for other thiol substrates. A paralog of CDO in mammals
was also identified and shown to be the other mammalian thiol dioxygenase, cysteamine dioxygenase (ADO). A tentative fingerprint
motif for ADOs, or DUF1637 family members, is proposed. In ADOs, the conserved glutamate residue in cupin motif 1 is replaced
by either glycine or valine. Both ADOs and CDOs appear to represent unique clades within the cupin superfamily. 相似文献
19.
Acrylamide (ACR) is a known industrial neurotoxic chemical that can induce neurodegeneration. Cytoskeletal protein aggregation is a pathological hallmark of neurodegenerative disorders. This study was an initial exploration on cytoskeletal proteins in plasma as potential biomarkers of ACR neurotoxicity. Low and high ACR groups received 20 mg/kg and 40 mg/kg ACR by intraperitoneal injection in adult Wistar rats and control group received physiological saline. Rats were all killed after 8 weeks to evaluate the levels of neurofilament(NF)-L, NF-M, NF-H, β-actin, α-tubulin, β-tubulin, tau, MAP2 proteins in plasma using both SDS-PAGE and western blotting. Compared with the control, the levels of NF-L, NF-M, NF-H, β-actin, tau, MAP2 proteins decreased and the level of α-tubulin increased in high ACR group, the levels of α-tubulin, β-tubulin and MAP2 increased in low ACR group. The results suggested that the changes of these proteins might be relevant to the neurotoxicity of ACR. Some of the cytoskeletal proteins in plasma might be used as marker of biological effect in ACR induced neuropathy. 相似文献
20.
To investigate the mechanisms of the axonopathy induced by 2,5-hexanedione (2,5-HD), male Wistar rats were administered at
a dosage of 400 mg/kg/day 2,5-HD (five times per week). The rats produced a slightly, moderately, or severely abnormal neurological
changes, respectively, after 2, 4, or 8 weeks of treatment. The cerebrums were Triton-extracted and ultracentrifuged to yield
a pellet fraction and a corresponding supernatant fraction. The relative levels of six cytoskeletal proteins (NF-L, NF-M,
NF-H, α-tubulin, β-tubulin, and β-actin) in both fractions were determined by immunoblotting. The results showed that NFs
content in HD-treated rats demonstrated a progressive decline as the intoxication of HD continued. As for microtubule proteins,
the levels of α-tubulin and β-tubulin demonstrated some inconsistent changes. The content of α-tubulin kept unchangeable,
while the content of β-tubulin increased significantly at the late stage of HD exposure. Furthermore, the content of β-actin
in both fractions remained unaffected throughout the study. These findings suggest that HD intoxication resulted in a progressive
decline of NFs, which was highly correlated with the development of HD-induced neuropathy. 相似文献