Table 1.

Production and Sequencing of Bovine EST Libraries

cDNA Library Tissue Collection animal % of RNA Fold normal Avg insert length (bp) No.of seq % GenBank nr match % Unique
MARC 1BOVMesenteric lymph node31818.31300 ± 63223,4701863
TIGR library ID: 2819Hilar lymph node318(n = 500)
Post-pubertal ovary418
Kidney-associated fat37
Hypothalamus318
Pituitary218
Subcutaneous fat33
MARC 2BOVTestis11516.81143 ± 59416,4942365
TIGR library ID: 2820Thymus216(n = 139)
Semitendenosous muscle215
Longissimus muscle216
Pancreas26
Adrenal gland216
Endometrium416
MARC 3BOVBone marrow22114.61188 ± 5646,1962382
TIGR library ID: 2821Alveolar macrophage320(n = 310)
Pre-pubertal ovary319
Fetal semitendonosous muscle520
Fetal longissimus muscle520
MARC 4BOVwhole embryos (pool of 4)d20 embryos5012.71008 ± 87922,3602060
TIGR library ID: 2822whole embryos (pool of 2)d40 embryos50(n = 232)
Total sequences68,520

[i] RNA from the indicated tissue was collected from one of five animals, with the exception of the d20 and d40 embryos which each represented a pool of embryos. The five animals used were (1) a 48-h-old Piedmontese-Angus cross calf, (2) a 20-d-old Simmental-MARCIII calf, (3) an 800-lb MARCIII yearling heifer, (4) a pregnant six-year-old Limousin cow, or (5) a d100 fetus from a Gelbvieh-Limousin cross. A pool of 5 ug of mRNA was used to construct each library, with percentage of the total amount of RNA from each tissue as indicated (% of RNA). Effective normalization of each library (fold normal) is expressed as the fold decrease in abundance of EF1a clones. The number of EST sequences deposited in GenBank from each library is indicated. Sequences were compared to GenBank nr database via BLASTanalysis, and percentage of clones showing significant match (score >300) is shown. The percentage of sequences with no significant overlap with other sequences from the same library is indicated (% unique).