Multisection T1-weighted hybrid-RARE: a pulse sequence for MR imaging of the entire liver during suspended respiration.

It is shown that the maximum average-data-collection-speed (ADCS) of multisection 2D hybrid-RARE sequences is independent of TR and TEeff, and a monotonically increasing function of echo-train-length (ETL). This result was used in the design of an optimized T1-weighted hybrid-RARE sequence that produces 20 images of the abdomen in 31 s divided into four breath-hold periods. The resulting ADCS is 58 lines in k-space per second. Twenty-four subjects (2 healthy volunteers and 22 patients) were imaged with a protocol that also included: (a) breath-hold T1-weighted FLASH which acquires data at 34 lines in k-space per second (49 s scan time), and (b) T1-weighted conventional spin-echo (9:44 minutes scan time) with respiratory compensation. The experiments show that this T1-weighted-hybrid-RARE sequence has: (1) a level of T1 weighting that is comparable with the conventional sequences, (2) very low vulnerability to susceptibility artifacts, (3) high data acquisition efficiency, and (4) higher SNR than T1-weighted-FLASH. In conclusion, the T1-weighted-hybrid-RARE sequence described herein is an efficacious and reproducible technique for rapid imaging of the upper abdomen during suspended respiration.

Partial characterization of chromosomal proteins tightly bound to chicken erythroid DNA.

Extraction of chicken reticulocyte and erythrocyte chromatins with 2 M NaCl yields a small fraction (about 5%) of the total DNA which is very tightly bound to a class of nonhistone chromatin proteins (DNA-P). This DNA fraction has previously been shown to be significantly enriched in active gene sequences. The proteins associated with reticulocyte and erythrocyte DNA-P were analyzed by two-dimensional gel electrophoresis. Reticulocyte DNA-P yield predominantly three major proteins, designated G1, G2, and G3 with relative masses of 80 000, 50 000, and 58 000, respectively. Erythrocyte DNA-P show only two proteins which appear to be similar to the reticulocyte G1 and G2 proteins, except in much reduced quantities as revealed by two-dimensional polyacrylamide gel electrophoresis. Amino acid analysis of the three reticulocyte proteins revealed that the ratio of acidic to basic amino acid residues increased in the order G1 less than G2 less than G3, while the respective isoelectric points also increased in that order.

Total poly(A+)-messenger RNA from bovine lens cofractionates with sucrose purified fiber cell plasma membrane.

Poly(A+)-messenger RNA was isolated from bovine lens as well as poly(A+)-mRNA from crude and sucrose-purified plasma membrane. Bovine lens MP26 antisera was also propagated in rabbits, from which anti-MP26 IgG was partially purified and used to assay for the specific synthesis of MP26 during in vitro translation of the isolated poly(A+)-mRNAs. We found that membrane-associated poly(A+)-mRNA supported the synthesis of proteins which were identical to those translated from total lens fiber cell poly(A+)-mRNA. These proteins included MP26, as assayed by immunoprecipitation of [35S]-labeled MP26.

Nuclear matrix DNA from chicken erythrocytes contains beta-globin gene sequences.

Nuclear matrices containing residual DNA were isolated from chicken erythrocytes after extraction of purified nuclei with buffered 2 M NaCl. After further purification of this residual DNA, it was found to contain high concentrations of beta-globin gene sequences as assayed by dot hybridization with 32P-labeled nick-translated pHB1001. Electron microscopy of a random sample of this residual DNA fraction shows the DNA to be intimately associated with protein at various intervals. A hypothesis for enrichment of active genes in residual DNA from purified chromatin or in nuclear matrix DNA is also discussed.