A A Lal
National Institutes of Health
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Featured researches published by A A Lal.
Molecular and Biochemical Parasitology | 1988
Thomas F. McCutchan; Vidal F. de la Cruz; A A Lal; John H. Gunderson; Hille J. Elwood; Mitchell L. Sogin
We have determined the complete sequence of two structurally distinct 18S ribosomal RNA genes from the malarial parasite Plasmodium falciparum. S1 nuclease analyses demonstrate that only one of the genes is represented in stable rRNA populations isolated from blood-stage parasites. Comparisons of homologous rRNA genes from Plasmodium berghei and P. falciparum reveal that they are identical at 86% of their positions. From comparisons of the Plasmodium genes to that of humans, it was possible to design genus-specific as well as species-specific oligonucleotide probes that can be used to distinguish the parasite 18S ribosomal RNA from that of its host. The utilization of these probes as diagnostic reagents is discussed.
Journal of Molecular Biology | 1984
Joël Vandekerckhove; A A Lal; Edward D. Korn
By amino acid sequence studies, only one form of cytoplasmic actin was detected in Acanthamoeba castellanii. Its amino acid sequence is very similar to the sequences of Dictyostelium and Physarum actins, from which Acanthamoeba actin differs in only nine and seven residues, respectively, including the deletion of the first residue. Acanthamoeba actin is unique in containing a blocked NH2-terminal neutral amino acid (glycine), while all other actins sequenced thus far have a blocked acidic amino acid (aspartic or glutamic) at the NH2 terminus. Acanthamoeba actin is also unique in that it contains an N epsilon-trimethyllysine residue at position 326. Like other actins, Acanthamoeba actin contains an NT-methylhistidine residue at position 73. The protein sequence is in complete agreement with the sequence derived from the nucleotide sequence of an expressed actin gene.
Molecular and Biochemical Parasitology | 1988
Vidal F. de la Cruz; A A Lal; Thomas F. McCutchan
We investigated the effect of long term passage of parasites in naive animals on the circumsporozoite protein (CSP) gene of Plasmodium yoelii. The CSP gene sequence was determined from a non-lethal cloned line of P. yoelii and compared to the CSP gene sequence from a lethal strain of P. yoelii. The two parasite lines were originally derived from the same isolate, but were separated 17 years ago followed by continued passage. The sequence of the CSP gene and its surroundings from the non-lethal line remains identical to that from the lethal isolate except for a deletion within the repeated central domain. This result contrasts with the results obtained by sequencing a number of clones from different geographical field isolates of Plasmodium falciparum where there appears to be rapid accumulation of sense mutations within putative functional domains. These observations are consistent with the suggestion that strong biological pressure in a field environment results in selection of parasite types on the basis of different CSP gene sequences.
Journal of Biological Chemistry | 1988
V F de la Cruz; A A Lal; Thomas F. McCutchan
Journal of Experimental Medicine | 1988
R D Adam; A Aggarwal; A A Lal; V F de La Cruz; Thomas F. McCutchan; Theodore E. Nash
Journal of Biological Chemistry | 1987
V F de la Cruz; A A Lal; Thomas F. McCutchan
Science | 1985
Thomas F. McCutchan; A A Lal; Vf de la Cruz; L H Miller; W L Maloy; Y Charoenvit; Rl Beaudoin; P Guerry; R Wistar; Sl Hoffman
Journal of Biological Chemistry | 1987
A A Lal; V F de la Cruz; J A Welsh; Y Charoenvit; W L Maloy; Thomas F. McCutchan
Journal of Biological Chemistry | 1988
A A Lal; V F de la Cruz; William E. Collins; Gary H. Campbell; Patricia M. Procell; Thomas F. McCutchan
Biochemistry | 1986
A A Lal; Edward D. Korn