Search

Theoretical considerations and diverse empirical data from clinical, psycholinguistic, and developmental studies suggest that language comprehension processes are decomposable into separate subsystems, including distinct systems for semantic and grammatical processing. Here we report that event-related potentials (ERPs) to syntactically well-formed but semantically anomalous sentences produced a pattern of brain activity that is distinct in timing and distribution from the patterns elicited by syntactically deviant sentences, and further, that different types of syntactic deviance produced distinct ERP patterns. Forty right-handed young adults read sentences presented at 2 words/sec while ERPs were recorded from over several positions between and within the hemispheres. Half of the sentences were semantically and grammatically acceptable and were controls for the remainder, which contained sentence medial words that violated (1) semantic expectations, (2) phrase structure rules, or (3) WH-movement constraints on Specificity and (4) Subjacency. As in prior research, the semantic anomalies produced a negative potential, N400, that was bilaterally distributed and was largest over posterior regions. The phrase structure violations enhanced the N125 response over anterior regions of the left hemisphere, and elicited a negative response (300-500 msec) over temporal and parietal regions of the left hemisphere. Violations of Specificity constraints produced a slow negative potential, evident by 125 msec, that was also largest over anterior regions of the left hemisphere. Violations of Subjacency constraints elicited a broadly and symmetrically distributed positivity that onset around 200 msec. The distinct timing and distribution of these effects provide biological support for theories that distinguish between these types of grammatical rules and constraints and more generally for the proposal that semantic and grammatical processes are distinct subsystems within the language faculty.

SV40 DNA was methylated in vitro with prokaryotic or eukaryotic DNA cytosine-5-methyltransferases and the inhibition of transcription by methylation was studied in Xenopus oocytes. Methylation with the prokaryotic HhaI or HpaII methyltransferases did essentially not inhibit transcription of SV40. Methylation with a rat liver methyltransferase led only to minor inhibition of the SV40 early genes, but to a complete shut shut off of the SV40 late genes. Partial methylation showed that methylation of both, the regulatory region and the 5' end of the SV40 late genes, was necessary for the effect on transcription. The TK gene could be inactivated by eukaryotic methylation of either the promoter and the first 50 nucleotides of the gene or the 3' rest of the gene. Insertion of the SV40 enhancer, not containing methylatable CpGs, into the TK upstream region, had no influence on the inhibition of TK gene transcription by methylation.

Methylation of cytosine in the DNA inhibits the transcription by RNA polymerase II in higher eukaryotes, but has no influence on RNA polymerase I transcription. The effect on RNA polymerase III was unknown, so far. Two polymerase III genes: a type 1 5S rRNA gene and a type 2 tRNA gene were methylated in vitro with a purified eukaryotic DNA methyltransferase (EC2.1.1.37) and their transcription was analyzed in Xenopus oocytes. The 5S rRNA gene, an oocyte 5S rRNA gene from X. laevis which is subject to developmental inactivation, was not affected by methylation. Conversely, transcription of the tRNA gene was 80% inhibited by methylation with the eukaryotic methyltransferase. HhaI and HpaII methylation left its transcription unaffected.

A possible role of DNA methylation as a factor in HIV latency was studied by methylating a HIV1-LTR-CAT plasmid in vitro and measuring its expression after transfection on Vero cells. Methylation with a eukaryotic DNA methylase resulted in a 70% inhibition of chloramphenicol acetyltransferase expression, in the absence as well as in the presence of the HIV1 trans-activator protein TAT in the cell. A similar degree of transcription inhibition was obtained by methylation of the only Hpa II site at position-143 in the HIV1-LTR with the bacterial Hpa II methylase. In contrast to the effect by eukaryotic methylation, the inhibition by Hpa II methylation could be partially reversed by cotransfection of the TAT gene. The reason may lie in an about 40% demethylation at the Hpa II site which was concomitantly observed.

Two experiments which test predictions derived from the assumption that lexical access involves a search process are reported. In the first experiment, test items must be classified as ambiguous or unambiguous, and in the second experiment, they are classified according to their syntactic properties. In both experiments, it is shown that when the target of the search is a nonexistent entry, an exhaustive search is involved, even though the test items are words. Further, in these conditions, frequency of occurrence is no longer related to decision time, as it is in lexical decision experiments. It is concluded that the search model adequately explains the procedure whereby the most common meaning of a homograph is accessed, but that the less common meaning is accessed in some completely different manner.

Using B1, Y29/55 and AL2 monoclonal antibodies (MoAbs) to target Burkitt lymphoma (BL) cell lines, we defined optimal conditions to lyse, in the presence of baby rabbit complement, BL cells in excess bone marrow (BM). After the purging procedure, down to one residual BL cell in 10(6) normal ones was detectable with a liquid cell culture assay. Using a cocktail of three MoAbs, on five different cell lines were observed more than 4 log BL cell depletion in samples contaminated with 1% BL cells and only one failure of the procedure on 17 experiments. However, a sixth line was constantly resistant to the procedure.

Reaction times in a simultaneous visual matching task were obtained for four types of letter strings: high-frequency words, low-frequency words, orthographically legal nonwords, e.g., CRAWN, and random letter strings. Two findings supported the notion that the matching of word items involves lexical access. First, words were processed faster than legal nonwords, indicating that the analysis of words uses an additional source of information apart from the constraints imposed by orthographic rules. Second, high-frequency words were processed faster than low-frequency words, indicating lexical search. It is proposed that three levels of identification and comparison operate simultaneously in the matching task: at a word level, a letter cluster level, and a letter level. The results of a second experiment give some support to the idea that these levels operate for "different" items as well as "same" items. Whether familiarity effects will be observed for "different" items will depend on the amount of identification and comparison of the two letter strings which is necessary before a difference is detected.